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D-1-N-Boc-prolinamide

CAS No.
35150-07-3
Chemical Name:
D-1-N-Boc-prolinamide
Synonyms
BOC-PRO-NH2;(R)-tert-butyl 2-carbamoylpyrrolidine-1-carboxylate;1-Boc-D-proL;BOC-L-PRO-NH2;BOC-PYRD(2)-NH2;Boc-Proliniamide;BOC-L-PROLINAMIDE;Boc-D-Prolinamide;N-Boc-Prolinamide;BOC-D-PROLINEAMIDE
CBNumber:
CB8284602
Molecular Formula:
C10H18N2O3
Molecular Weight:
214.26
MDL Number:
MFCD00190827
MOL File:
35150-07-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:33:38

D-1-N-Boc-prolinamide Properties

Melting point 104-108 °C
Boiling point 370.1±31.0 °C(Predicted)
Density 1.155±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form powder to crystal
pka 15.97±0.20(Predicted)
color White to Almost white
optical activity Consistent with structure
Major Application peptide synthesis
InChI 1S/C10H18N2O3/c1-10(2,3)15-9(14)12-6-4-5-7(12)8(11)13/h7H,4-6H2,1-3H3,(H2,11,13)/t7-/m0/s1
InChIKey PITJAAIPVBVRAO-ZETCQYMHSA-N
SMILES CC(C)(C)OC(=O)N1CCC[C@H]1C(N)=O
CAS DataBase Reference 35150-07-3(CAS DataBase Reference)
UNSPSC Code 12352209
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312a-P330-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  22
Safety Statements  24/25
WGK Germany  2
HS Code  2933.99.9701
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
REACH Registrations Active
NFPA 704
1
2 0

D-1-N-Boc-prolinamide price More Price(67)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 661198 1-Boc-L-prolinamide 97% 35150-07-3 1g $69.5 2023-06-20 Buy
Sigma-Aldrich 661198 1-Boc-L-prolinamide 97% 35150-07-3 5g $323 2023-06-20 Buy
TCI Chemical B3756 N-(tert-Butoxycarbonyl)-L-prolinamide >98.0%(HPLC)(N) 35150-07-3 1g $24 2026-04-30 Buy
TCI Chemical B3756 N-(tert-Butoxycarbonyl)-L-prolinamide >98.0%(HPLC)(N) 35150-07-3 5g $31 2026-04-30 Buy
Usbiological 409028 1-Boc-L-Prolinamide 35150-07-3 100mg $312 2026-06-03 Buy
Product number Packaging Price Buy
661198 1g $69.5 Buy
661198 5g $323 Buy
B3756 1g $24 Buy
B3756 5g $31 Buy
409028 100mg $312 Buy

D-1-N-Boc-prolinamide Chemical Properties, Uses, Production

Chemical Properties

White to off-white powder

Uses

1-Boc-L-prolinamide is a reagent that is used in the preparation of thiazole amide peptidomimetics as erratum inhibitor apoptosis protein antagonist.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

BOC-L-Proline

15761-39-4

D-1-N-Boc-prolinamide

35150-07-3

GENERAL METHOD: BOC-L-proline (1.00 g, 4.65 mmol), di-tert-butyl dicarbonate (1.52 g, 6.97 mmol), ammonium bicarbonate (0.55 g, 6.97 mmol), and pyridine (1.0 mL) were dissolved in dioxane (20 mL), and the reaction was stirred at room temperature for 6 hours. After completion of the reaction, the product was extracted with dichloromethane, the organic phase was washed sequentially with 1 M hydrochloric acid and saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. To the concentrate was added n-hexane (100 mL) and sonication prompted the product to precipitate as a white solid to afford N-tert-butoxycarbonyl-L-prolinamide (0.85 g, 85% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 4.37-4.34 (m, 1H), 3.47-3.36 (m, 2H), 2.07-1.85 (m, 4H), 1.49 (s, 9H). Mass spectrum (ESI) m/z 215 [M + H]+.

References

[1] Bioorganic and Medicinal Chemistry, 2002, vol. 10, # 6, p. 1719 - 1729
[2] Canadian Journal of Chemistry, 2007, vol. 85, # 2, p. 85 - 95
[3] Journal of Agricultural and Food Chemistry, 2012, vol. 60, # 35, p. 8544 - 8551
[4] Journal of Medicinal Chemistry, 2017, vol. 60, # 1, p. 228 - 247
[5] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 23, p. 7418 - 7429

15761-39-4
35150-07-3
Synthesis of D-1-N-Boc-prolinamide from BOC-L-Proline

D-1-N-Boc-prolinamide Preparation Products And Raw materials

Global Suppliers ( 302)
Supplier Tel Email Country ProdList Advantage
Shanghai Boyle Chemical Co., Ltd. 021-50182298 021-50180596 sales@boylechem.com China 2202 55
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Wuhan Chemwish Technology Co., Ltd 86-027-67849912 sales@chemwish.com China 35884 56
GL Biochem (Shanghai) Ltd 21-61263452 13641803416 ymbetter@glbiochem.com China 9981 64
Capot Chemical Co., Ltd +86 (0) 571 85 58 67 18 China 18187 66
Shanghai Sinch Parmaceuticals Tech. Co. Ltd. +86-21-54098501 sales@sinch.com.cn China 11592 64

View Latest Price from D-1-N-Boc-prolinamide manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
D-1-N-Boc-prolinamide pictures 2019-07-06 D-1-N-Boc-prolinamide
35150-07-3
$100.00 1KG 99% Career Henan Chemical Co

D-1-N-Boc-prolinamide Spectrum

BOC-L-PROLINAMIDE BOC-L-PRO-NH2 BOC-L-PROLINE AMIDE BOC-PYRD(2)-NH2 L-1-N-Bocprolidinamid tert-butyl (2S)-2-carbamoylpyrrolidine-1-carboxylate 1-Pyrrolidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester, (2S)- N-Boc-L-Prolinamide (S)-N-BOC-Pyrrolidine-2-carboxamide Vildagliptin Impurity 16 (S)-Boc-pyrrolidine-2-carboxylic acid amide Boc-L-proline amide≥ 99% (HPLC) N-Boc-L-prolinamide,99%e.e. tert-Butyl (S)-2-carbamoylpyrrolidine-1-carboxylate (Tert-Butoxy)Carbonyl Pro-NH2 L-1-N-BOC-PROLIDINAMIDE (L)-1-N-BOC-PROLINAMIDE Boc-D-Prolinamide D-1-N-Boc-prolinamide tert-Butyl (2R)-2-carbamoylpyrrolidine-1-carboxylate 1-BOC-L-PROLINAMIDE (S)-2-(AMINOCARBONYL)-1-PYRROLIDINECARBOXYLIC ACID, 1,1-DIMETHYLETHYL ESTER (S)-2-CARBAMOYL-PYRROLIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER N-ALPHA-T-BUTYLOXYCARBONYL-L-PROLINE AMIDE N-ALPHA-T-BUTOXYCARBONYL-L-PYRROLIDINE-2-CARBOXYLIC ACID AMIDE N-ALPHA-T-BUTOXYCARBONYL-L-PROLINE AMIDE N-ALPHA-TERT-BUTYLOXYCARBONYL-L-PROLINE AMIDE N-(TERT-BUTOXYCARBONYL)PROLINE AMIDE N-TERT-BUTOXYCARBONYL-L-PROLINE AMIDE DL-1-BOC-PROLINAMIDE N-alpha-t-Butyloxycarbonyl-D-proline amide N-ALPHA-BOC-L-PROLINEAMIDE BOC-D-PROLINEAMIDE N-(tert-Butoxycarbonyl)proline amide, (S)-2-(Aminocarbonyl)-1-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester N-(tert-Butoxycarbonyl)-L-prolinaMide Boc-Proliniamide N-(tert-Butoxycarbonyl)-L-prolinamide > 1-Boc-D-proL (S)-2-Carbamoyl-1-pyrrolidinecarboxylic Acid tert-Butyl Ester tert-Butyl (S)-2-Carbamoyl-1-pyrrolidinecarboxylate D-1-N-Boc-prolinamide USP/EP/BP N-Boc-Prolinamide BOC-L-Prolinamide extrapure, 98% 1,1-Dimethylethyl (2S)-2-(aminocarbonyl)-1-pyrrolidinecarboxylate 1-Boc-L-prolinamide (R)-tert-butyl 2-carbamoylpyrrolidine-1-carboxylate BOC-PRO-NH2 DL-Asparagine monohydrat 35150-07-3 C10H18N2O3 Amino Acid Derivatives Amino Acids Pyrrole&Pyrrolidine&Pyrroline