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(2S)-Bornane-10,2-sultam

(2S)-Bornane-10,2-sultam Structure
(2S)-Bornane-10,2-sultam structure
CAS No.
108448-77-7
Chemical Name:
(2S)-Bornane-10,2-sultam
Synonyms
(+)-10,2-CAMPHORSULTAM;2-sultaM;(+)-10,2-Camphorsultam;(7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide;L-SultaM;(2S)-Bornane-10;L-2,10-amphorsultam;D-(-)-CAMPHOR SULTAM;(2S)-Borne-10,2-sultam;(1R)-(+)-Camphorsultam
CBNumber:
CB2411257
Molecular Formula:
C10H17NO2S
Molecular Weight:
215.31
MDL Number:
MFCD00151762
MOL File:
108448-77-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:35:56
Product description Number Pack Size Price
(+)-10,2-Camphorsultam >98.0%(GC) C1324 1g $94
(+)-10,2-Camphorsultam >98.0%(GC) C1324 5g $325
(+)-10,2-Camphorsultam Asreported 270510 500mg $306
(+)-10,2-Camphorsultam Asreported 270510 1g $420
(+)-10,2-Camphorsultam Asreported 270510 2g $568
More product size
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(2S)-Bornane-10,2-sultam Properties

Melting point 185-187 °C(lit.)
alpha 33 º (c=4.9, CHCl3)
Boiling point 324.8±25.0 °C(Predicted)
Density 1.1469 (rough estimate)
refractive index 31 ° (C=1, CHCl3)
storage temp. Sealed in dry,Room Temperature
solubility almost transparency in Chloroform
pka 11.05±0.40(Predicted)
form powder to crystal
color White to Almost white
optical activity [α]20/D +32°, c = 5 in chloroform
BRN 4675755
InChI InChI=1S/C10H17NO2S/c1-9(2)7-3-4-10(9)6-14(12,13)11-8(10)5-7/h7-8,11H,3-6H2,1-2H3/t7-,8-,10-/m0/s1
InChIKey DPJYJNYYDJOJNO-CFGJQEBVSA-N
SMILES N1[C@]2([H])[C@@]3(C(C)(C)[C@]([H])(C2)CC3)CS1(=O)=O
CAS DataBase Reference 108448-77-7(CAS DataBase Reference)
UNSPSC Code 12352005

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P280a-P304+P340-P405-P501a-P261-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
HS Code  29242990
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

(2S)-Bornane-10,2-sultam price More Price(61)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical C1324 (+)-10,2-Camphorsultam >98.0%(GC) 108448-77-7 1g $94 2021-12-16 Buy
TCI Chemical C1324 (+)-10,2-Camphorsultam >98.0%(GC) 108448-77-7 5g $325 2026-04-30 Buy
Usbiological 270510 (+)-10,2-Camphorsultam Asreported 108448-77-7 500mg $306 2026-06-03 Buy
Usbiological 270510 (+)-10,2-Camphorsultam Asreported 108448-77-7 1g $420 2026-06-03 Buy
Usbiological 270510 (+)-10,2-Camphorsultam Asreported 108448-77-7 2g $568 2026-06-03 Buy
Product number Packaging Price Buy
C1324 1g $94 Buy
C1324 5g $325 Buy
270510 500mg $306 Buy
270510 1g $420 Buy
270510 2g $568 Buy

(2S)-Bornane-10,2-sultam Chemical Properties,Uses,Production

Chemical Properties

white to light yellow crystal powde

Uses

(1R)-(+)-2,10-Camphorsultam has been used as a reactant in the synthesis of pyrrolidine acid analogs as potent dual PPARα/γ agonists.

Application

(2S)-Bornane-10,2-sultam is a pharmaceutical intermediate compound that can be used to synthesize sulfonamide drugs.  (2R)-Bornane-10,2-sultam can be used as a chiral auxiliary to perform intramolecular 1,3-dipolar cycloadditions to generate bridged and fused cycloadditions with complete diastereocontrol.  Reduction of fused isoxazolidines can generate 1-azaspiro[4.5]decane, which is a potential intermediate in the asymmetric synthesis of cylindrosin alkaloids[1].

Purification Methods

The (-)-enantiomer is recrystallised from 95% EtOH and dried in a vacuum desiccator. It dissolves in dilute aqueous NaOH and can be precipitated without hydrolysis by acidifying. It forms the N-Na salt in EtOH (by addition of Na to the EtOH solution), and the salt can be methylated with MeI to give the (-)-N-Me lactam with m 80o after recrystallisation from hot H2O and has []D -59.6o (c 5, CHCl3) [Shriner et al. J Am Chem Soc 60 2794 1938]. [Oppolzer et al. Helv Chim Acta 69 1142 1986, Weismiller et al. Org Synth 69 154 1955, Beilstein 27 III/IV 1007.]

References

[1] MARK C BAGLEY; Wolfgang O. Asymmetric synthesis of 1-azaspiro[4.5]decanes via intramolecular dipolar cycloaddition of nitrones containing the bornane-10,2-sultam chiral auxiliary[J]. Tetrahedron, asymmetry, 2000. DOI:10.1016/S0957-4166(00)00205-6.

(2S)-Bornane-10,2-sultam synthesis

107869-45-4
108448-77-7
Synthesis of (2S)-Bornane-10,2-sultam from (+)-10-CAMPHORSULFONIMINE

(2S)-Bornane-10,2-sultam Preparation Products And Raw materials

Raw materials

Preparation Products

(+)-10-CAMPHORSULFONIMINE

(2S)-Bornane-10,2-sultam Suppliers

Global( 281)Suppliers
Supplier Tel Email Country ProdList Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd
+86-51982698291; +86-15295095616 info@hhbhswkj.com China 131 58
Accendatech Co., Ltd.
+undefined+86-13132578992 yunhao.liu@accendatech.com China 250 58
Capot Chemical Co.,Ltd. 		+86-（0）57185586718 +86-13336195806 sales@capot.com China 29626 60
Shanghai Daken Advanced Materials Co.,Ltd 		+86-2158073036 info@dakenam.com China 14036 58
ATK CHEMICAL COMPANY LIMITED 		+undefined-21-51877795 ivan@atkchemical.com China 32997 60
career henan chemical co 		+86-0371-86658258 sales@coreychem.com China 29766 58
Alchem Pharmtech,Inc. 		8485655694 sales@alchempharmtech.com United States 63645 58
CONIER CHEM AND PHARMA LIMITED 		sales@conier.com China 49906 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd 		+8613580539051 joe@yuhengpharm.com CHINA 21135 58
SIMAGCHEM CORP 		+86-5922680277 +86-13806087780 sale@simagchem.com China 17339 58
Supplier Advantage
Changzhou Chontech Baocheng Chemical Co.,Ltd
58
Accendatech Co., Ltd.
58
Capot Chemical Co.,Ltd. 		60
Shanghai Daken Advanced Materials Co.,Ltd 		58
ATK CHEMICAL COMPANY LIMITED 		60
career henan chemical co 		58
Alchem Pharmtech,Inc. 		58
CONIER CHEM AND PHARMA LIMITED 		58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd 		58
SIMAGCHEM CORP 		58

View Lastest Price from (2S)-Bornane-10,2-sultam manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(1R)-(+)-2,10-Camphorsultam pictures 2026-08-16 (1R)-(+)-2,10-Camphorsultam
108448-77-7
 $1.00 1g 99% 20tons Zibo Hangyu Biotechnology Development Co., Ltd
(2S)-Bornane-10,2-sultam pictures 2025-11-18 (2S)-Bornane-10,2-sultam
108448-77-7
 $1.10 1g 99.00% 100 Tons Min Dideu Industries Group Limited
(1R)-(+)-2,10-Camphorsultam pictures 2023-02-18 (1R)-(+)-2,10-Camphorsultam
108448-77-7
 1kg 98% Aromsyn Co., Ltd.

(2S)-Bornane-10,2-sultam Spectrum

(2S)-Bornane-10,2-sultam(108448-77-7)MS(2S)-Bornane-10,2-sultam(108448-77-7)1HNMR(2S)-Bornane-10,2-sultam(108448-77-7)13CNMR(2S)-Bornane-10,2-sultam(108448-77-7)IR1(2S)-Bornane-10,2-sultam(108448-77-7)IR2(2S)-Bornane-10,2-sultam(108448-77-7)Raman

108448-77-7((2S)-Bornane-10,2-sultam)Related Search:

3-Aminobenzenesulfonamide Dacthal Dimethyl ether Methanesulfonamide Cyclopropanesulfonamide
Dimethyl fumarate Benzenesulfonamide Dimethyl carbonate ETHANE Dimethyl sulfate
Dimethyl phthalate Dimethyl disulfide p-Toluenesulfonamide Dimethyl sulfoxide Sulfanilamide
N,N-Dimethylformamide (2R)-Bornane-10,2-sultam (1S)-(+)-10-CAMPHORSULFONAMIDE

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(7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide (2S)-Borne-10,2-sultam L-2,10-Camphorsultam,99%e.e. (2S)-BORNANE-10,2-SULTAM (1R)-(+)-2,10-CAMPHORSULTAM (1R)-2,10-CAMPHORSULTAM (1R,2S)-(+)-2,10-CAMPHORSULTAM (1R,5S)-10,10-DIMETHYL-3-THIA-4-AZATRICYCLO[5.2.1.01,5]DECANE 3,3-DIOXIDE (IR)-(+)-2,10-Camphorsultam (1R)-(+)-2,10-camphorsultam ,98% L-2,10-amphorsultam (2S)-Bornane-10 (2S)-Bornane-1,2-sultaM L-SultaM (2S)-Bornane-10,2-sultam (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.0(1,5)]decane 3,3-Dioxide (1R)-(+)-2,10-Camphorsultam (5S,7S)-10,10-dimethyl-3λ-thia-4-azatricyclo[5.2.1.01,]decane-3,3-dione (2S)-Bornane-10,2-sultam (1R)-(+)-2,10-Camphorsultam [3AR-(3A-ALPHA,6-ALPHA,7A-BETA)]-HEXAHYDRO-8,8-DIMETHYL-2,2-DIOXIDE-3H-3A,6-METHANO-2,1-BENZISOTHIAZOLE [3aR-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-2,2-dioxide-3H-3a,6-methano-2,1-benzisothiazole (+)-EXO-10,2-BORNANESULTAM (+)-L-2,10-CAMPHORSULTAM L(+)-10,2-CAMPHORSULTAME D-(-)-CAMPHOR SULTAM (+)-2,10-CAMPHORSULTAM 99% (2S)-Bornane-10,2-sultam,99+%, (99+% ee) (2S)-Bornane-10,2-sultam,98% (+)-exo-10,2-Bornanesultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide (+)-10,2-Camphorsultam, (+)-exo-10,2-Bornanesultam, L-2,10-Camphorsultam, (1R,5S)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane 3,3-dioxide (1β,5α,7β)-10,10-Dimethyl-3-thia-4-azatricyclo[5.2.1.01,5]decane3,3-dioxide (3aR)-1,4,5,6,7,7aβ-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide (3aR,3aα,6α,7aβ)-8,8-Dimethyl-3a,6-methanooctahydro-2,1-benzisothiazole 2,2-dioxide [3aR,7aβ,(+)]-Hexahydro-8,8-dimethyl-3H-3aα,6α-methano-2,1-benzisothiazole 2,2-dioxide (1R)-(+)-Camphorsultam (1R,2S)-(+)-10,2-Camphorsultam (1R,2S)-(+)-10,2-CamphorsuL 3H-3a,6-Methano-2,1-benzisothiazole, hexahydro-8,8-dimethyl-, 2,2-dioxide, (3aR,6S,7aS)- (3aR)-8,8-dimethylhexahydro-2H-3a,6-methanobenzo[d]isothiazole 1,1-dioxide (2S)-Bornane-10,2-sultam ISO 9001：2015 REACH (3aR,6S,7aS)-8,8-Dimethylhexahydro-1H-3a,6-methanobenzo[c]isothiazole 2,2-dioxide (5S,7S)-10,10-dimethyl-3λ?-thia-4-azatricyclo[5.2.1.01?]decane 3,3-dioxide (+)-2,10-Camphorsultam L-(+)-Camphor sulfonamide (+)-10,2-Camphorsultam (+)-10,2-CAMPHORSULTAM 2-sultaM 108448-77-7 C10H17NO2S Sulfur-Based Sulfur Compounds (for Synthesis) Bicyclic Monoterpenes Terpenes Asymmetric Synthesis Chiral Auxiliaries chiral Asymmetric Synthesis Bicyclic Monoterpenes Biochemistry