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N-(3-BROMOPROPYL)PHTHALIMIDE

CAS No.
5460-29-7
Chemical Name:
N-(3-BROMOPROPYL)PHTHALIMIDE
Synonyms
2-(3-BROMO-PROPYL)-ISOINDOLE-1,3-DIONE;2-(3-BroMopropyl)isoindoline-1.3-dione;AKOS 226-47;AURORA KA-570;TIMTEC-BB SBB003049;LABOTEST-BB LT00455358;(3-bromopropyl)phthalimide;N-(3-Bromopropyl)phthahmide;N-(3-bromopropyl)pthalimide;N-(3-BROMOPROPYL)PHTHALIMIDE
CBNumber:
CB2237116
Molecular Formula:
C11H10BrNO2
Molecular Weight:
268.11
MDL Number:
MFCD00005904
MOL File:
5460-29-7.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:02:13
Product description Number Pack Size Price
N-(3-Bromopropyl)phthalimide 98% B80003 25g $52.9
N-(3-Bromopropyl)phthalimide 98% B80003 100g $128
N-(3-Bromopropyl)phthalimide >98.0%(HPLC)(N) B1328 25g $58
N-(3-Bromopropyl)phthalimide >98.0%(HPLC)(N) B1328 500g $619
N-(3-Bromoprop-1-yl)phthalimide 4H18-9-23 500g $495
More product size

N-(3-BROMOPROPYL)PHTHALIMIDE Properties

Melting point 72-74 °C(lit.)
Boiling point 361℃
Density 1.578
refractive index 1.6320 (estimate)
Flash point 172℃
storage temp. Inert atmosphere,Room Temperature
solubility <1g/l
form Crystalline Powder or Crystals
pka -2.21±0.20(Predicted)
color White to light beige
BRN 157547
InChI InChI=1S/C11H10BrNO2/c12-6-3-7-13-10(14)8-4-1-2-5-9(8)11(13)15/h1-2,4-5H,3,6-7H2
InChIKey VKJCJJYNVIYVQR-UHFFFAOYSA-N
SMILES C1(=O)C2=C(C=CC=C2)C(=O)N1CCCBr
CAS DataBase Reference 5460-29-7(CAS DataBase Reference)
FDA UNII VQG2G776PS
UNSPSC Code 12352111
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
Risk Statements  36/37/38
Safety Statements  22-24/25
WGK Germany  3
HS Code  29251900
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

N-(3-BROMOPROPYL)PHTHALIMIDE price More Price(65)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich B80003 N-(3-Bromopropyl)phthalimide 98% 5460-29-7 25g $52.9 2026-04-30 Buy
Sigma-Aldrich B80003 N-(3-Bromopropyl)phthalimide 98% 5460-29-7 100g $128 2026-04-30 Buy
TCI Chemical B1328 N-(3-Bromopropyl)phthalimide >98.0%(HPLC)(N) 5460-29-7 25g $58 2026-04-30 Buy
TCI Chemical B1328 N-(3-Bromopropyl)phthalimide >98.0%(HPLC)(N) 5460-29-7 500g $619 2026-04-30 Buy
SynQuest Laboratories 4H18-9-23 N-(3-Bromoprop-1-yl)phthalimide 5460-29-7 500g $495 2026-05-22 Buy
Product number Packaging Price Buy
B80003 25g $52.9 Buy
B80003 100g $128 Buy
B1328 25g $58 Buy
B1328 500g $619 Buy
4H18-9-23 500g $495 Buy

N-(3-BROMOPROPYL)PHTHALIMIDE Chemical Properties,Uses,Production

Chemical Properties

white powder

Uses

N-(3-Bromopropyl)phthalimide is used in synthesis of several organic compounds including that of flavonoid derivatives which act as selective ABCC1 modulators with potential use as pharmacological tools for investigation of the role of ABCC1. It is also used in the synthesis of Hederagenin which is a triterpene template for the development of new antitumor compounds.

reaction suitability

reagent type: cross-linking reagent

Synthesis

Potassium phthalimide

1074-82-4

1,3-Dibromopropane

109-64-8

N-(3-BROMOPROPYL)PHTHALIMIDE

5460-29-7

In 50 mL of DMF, 0.025 mol of phthalimide potassium salt, 0.10 mol of 1,3-dibromopropane and 0.5 g of TBAB were added and the reaction was carried out at 70°C for 2.0 hours. After completion of the reaction, the mixture was cooled to room temperature, poured into ice water and extracted with ethyl acetate. The organic phase was sequentially washed with water, dried, concentrated and allowed to stand overnight to give 5.91 g of N-(3-bromopropyl)phthalimide as a white solid with a melting point of 70-73°C and a yield of 88.3%.

Purification Methods

Place it in a Soxhlet and extract it with Et2O, whereby the bis-phthalimido impurity is not extracted. Evaporate the Et2O and recrystallise the residue from EtOH, aqueous EtOH or pet ether. [Gabriel & Weiner Chem Ber 21 2669 1888, Gaudry Can J Chem 31 1060 1953, Beilstein 21/10 V 1277.]

References

[1] Patent: CN107382980, 2017, A. Location in patent: Paragraph 0035; 0036; 0037; 0038
[2] Patent: CN107540647, 2018, A. Location in patent: Paragraph 0049-0051
[3] European Journal of Medicinal Chemistry, 2018, vol. 149, p. 69 - 78
[4] Chemistry - A European Journal, 2014, vol. 20, # 6, p. 1530 - 1538
[5] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 7, p. 1223 - 1227

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View Lastest Price from N-(3-BROMOPROPYL)PHTHALIMIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
N-(3-bromopropyl)phthalimide pictures 2026-05-21 N-(3-bromopropyl)phthalimide
5460-29-7
25kgs/paper drum 98% 50 tons YiZheng HaiFan Chemical CO., LTD.
N-(3-Bromopropyl)phthalimide pictures 2026-04-17 N-(3-Bromopropyl)phthalimide
5460-29-7
$3.00-9.00 99% ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
N-(3-BROMOPROPYL)PHTHALIMIDE pictures 2026-03-20 N-(3-BROMOPROPYL)PHTHALIMIDE
5460-29-7
1KG 99% 20 mt Hebei Chuanghai Biotechnology Co., Ltd
AURORA KA-570 GAMMA-BROMOPROPYLPHTHALIMIDE LABOTEST-BB LT00455358 2-(3-BROMO-PROPYL)-ISOINDOLE-1,3-DIONE 2-(3-BROMOPROPYL)-1H-ISOINDOLE-1,3(2H)-DIONE AKOS 226-47 TIMTEC-BB SBB003049 N-(3-BROMOPROPYL)PHTHALIMIDE 2-(3-Bromoprop-1-yl)-1H-isoindole-1,3(2H)-dione, 2-(3-Bromoprop-1-yl)isoindoline-1,3-dione N-(3-Bromoprop-1-yl)phthalimide 1-Phthalimido-3-bromopropane 2-(3-Bromopropyl)-1H-isoindol-1,3(2H)-dione N-(3-BroMopropyl)phthaliMide, 98% 25GR N-(3-BROMOPROPYL)PHTHALIMIDE FOR SYNTHES 2-(BroMopropyl)-1,3-dihydro-1,3-dioxoisoindole N-(3-BroMopropyl)phthaliMide 98% N-(3-Bromopropyl)phthahmide BROMOPROPYLPHTHALIMIDEN3()-- N-(3-Bromopropyl)-Phthalimide~97% N-(3-Bromopropyl)phthalimide,98% 1H-Isoindole-1,3(2H)-dione, 2-(3-bromopropyl)- (3-bromopropyl)phthalimide N-(3-bromopropyl)pthalimide 2-(3-bromopropyl)isoindoline-1,3-dione hydrochloride N-(3-Bromopropyl)phthalimide > Dimethyl 26-bromo terephthalate N-(3-Bromopropyl)phthalimide 2-(3-BroMopropyl)isoindoline-1.3-dione 5460-29-7 N-Substituted Phthalimides N-Substituted Maleimides, Succinimides & Phthalimides AMINE Cyclic Imides Organic Building Blocks Building Blocks Carbonyl Compounds alkyl bromide N-Substituted Maleimides, Succinimides & Phthalimides N-Substituted Phthalimides Bifunctional CrosslinkersOrganic Building Blocks Carbonyl Compounds Cyclic Imides Linkers Peptide Synthesis