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4-Bromo-benzamidine

CAS No.
22265-36-7
Chemical Name:
4-Bromo-benzamidine
Synonyms
p-Bromobenzamidine;4-Bromo-benzamidine;4-bromobenzammidine;CHEMBRDG-BB 4012620;4-BROMOBENZAMIDINE HCL;4-BroMo-benzaMidine HCl salt;4-Bromobenzenecarboximidamide;BenzenecarboxiMidaMide, 4-broMo-;4-bromobenzenecarboximidamide 1HCl;4-BROMOBENZENECARBOXIMIDAMIDE HYDROCHLORIDE
CBNumber:
CB7230107
Molecular Formula:
C7H7BrN2
Molecular Weight:
199.05
MDL Number:
MFCD05662836
MOL File:
22265-36-7.mol
MSDS File:
SDS
Last updated:2026-09-12 18:54:48

4-Bromo-benzamidine Properties

Melting point 218℃
Boiling point 261℃
Density 1.62
Flash point 112℃
storage temp. Sealed in dry,Room Temperature
pka 11.39±0.50(Predicted)

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

4-Bromo-benzamidine price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS118571 4-Bromobenzimidamide 95% 22265-36-7 1g $50 2026-06-04 Buy
Activate Scientific AS118571 4-Bromobenzimidamide 95% 22265-36-7 5g $179 2026-06-04 Buy
Activate Scientific AS118571 4-Bromobenzimidamide 95% 22265-36-7 25g $505 2026-06-04 Buy
Synthonix B45615 4-Bromobenzimidamide 95+% 22265-36-7 250mg $61.6 2026-05-06 Buy
Synthonix B45615 4-Bromobenzimidamide 95+% 22265-36-7 1g $90 2026-05-06 Buy
Product number Packaging Price Buy
AS118571 1g $50 Buy
AS118571 5g $179 Buy
AS118571 25g $505 Buy
B45615 250mg $61.6 Buy
B45615 1g $90 Buy

4-Bromo-benzamidine Chemical Properties,Uses,Production

Synthesis

4-Bromobenzamidine hydrochloride

55368-42-8

4-BROMO-BENZAMIDINE

22265-36-7

The general procedure for the synthesis of 4-bromobenzamidine hydrochloride from 4-bromobenzamidine hydrochloride was as follows: first, 4-bromobenzamidine hydrochloride (6a, 707 mg) was treated with 5 M aqueous sodium hydroxide (8 mL), followed by extraction with chloroform. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give a colorless solid (472 mg). Next, the resulting solid was dissolved in ethanol (5 mL), ethyl propargylate (0.27 mL) was added and the reaction mixture was heated to 60 °C. Then, a solution of potassium hydroxide (175 mg) in ethanol (4 mL) was added dropwise over 15 minutes. The reaction mixture was further heated to 80 °C and stirred at this temperature for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature, acidified by addition of 1 M hydrochloric acid (10 mL) and the precipitate was collected by filtration. The precipitate was washed with water and dried under vacuum at 50 °C overnight to give 7 g (267 mg, 35% yield) of the target product as a light brown solid. The product was characterized by 1H NMR (DMSO-d6): δ 6.25-5.50 (1H, m), 7.74 (2H, d, J = 8.3 Hz), 7.95-8.25 (3H, m), 12.50-13.20 (1H, br); FAB-MS m/z 251,253 [(M + H)+].

References

[1] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 7, p. 2369 - 2375
[2] Patent: EP2862856, 2015, A1. Location in patent: Paragraph 0651; 0652
[3] Tetrahedron Letters, 2018, vol. 59, # 4, p. 361 - 364

4-Bromo-benzamidine Preparation Products And Raw materials

Global( 58)Suppliers
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J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
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SanoChem (Chengdu) Tech. Co., Ltd. 28-87999436 02887999436 sales@sano-chem.com China 3792 55
CHEMBRDG-BB 4012620 4-BROMOBENZENECARBOXIMIDAMIDE HYDROCHLORIDE 4-bromobenzammidine 4-bromobenzenecarboximidamide(SALTDATA: HCl) 4-bromobenzenecarboximidamide 1HCl p-Bromobenzamidine 4-BroMo-benzaMidine HCl salt BenzenecarboxiMidaMide, 4-broMo- 4-BROMOBENZAMIDINE HCL 4-Bromobenzenecarboximidamide 4-Bromo-benzamidine 22265-36-7 pharmacetical