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N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde

CAS No.
143722-29-6
Chemical Name:
N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde
Synonyms
Butanoicacid,4-chloro-6-oxo-;1-(1H-1,3-BENZODIAZOL-2-YL)-1H-PYRAZOL-7-AMINE;1-(4-bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde;N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde;3-[(4-Bromophenyl)methyl]-2-butyl-5-chloroimidazole-4-carbaldehyde;1-[(4-BroMophenyl)Methyl]-2-butyl-4-chloro-1H-iMidazole-5-carboxaldehyde;1H-Imidazole-5-carboxaldehyde, 1-[(4-bromophenyl)methyl]-2-butyl-4-chloro-
CBNumber:
CB62503134
Molecular Formula:
C15H16BrClN2O
Molecular Weight:
355.66
MDL Number:
MFCD18382199
MOL File:
143722-29-6.mol
MSDS File:
SDS
Last updated:2026-05-28 02:27:10
Product description Number Pack Size Price
N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% AA001I7I 250mg $74
N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% AA001I7I 1g $174
N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% AA001I7I 5g $507
1-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 97% CD11257030 100mg $89
1-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 97% CD11257030 250mg $143

N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde Properties

storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Chloroform, Dichloromethane, Ethyl Acetate, Methanol

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

N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
aablocks AA001I7I N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% 143722-29-6 250mg $74 2026-05-28 Buy
aablocks AA001I7I N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% 143722-29-6 1g $174 2026-05-28 Buy
aablocks AA001I7I N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 95% 143722-29-6 5g $507 2026-05-28 Buy
Crysdot CD11257030 1-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 97% 143722-29-6 100mg $89 2026-05-26 Buy
Crysdot CD11257030 1-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 97% 143722-29-6 250mg $143 2026-05-26 Buy
Product number Packaging Price Buy
AA001I7I 250mg $74 Buy
AA001I7I 1g $174 Buy
AA001I7I 5g $507 Buy
CD11257030 100mg $89 Buy
CD11257030 250mg $143 Buy

N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde Chemical Properties,Uses,Production

Uses

Intermediate in the production of Sartan derivatives

Synthesis

2-Butyl-4-chloro-5-formylimidazole

83857-96-9

4-Bromobenzyl bromide

589-15-1

N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde

143722-29-6

Example 14 Synthesis of 1-(4-bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 2-n-butyl-4-chloro-1H-imidazole-5-carboxaldehyde (111.9 g, 0.6 mol), p-bromobenzyl bromide (153.02 g, 0.6 mol), anhydrous potassium carbonate (103.5 g, 0.75 mol), and dry N,N-dimethylacetamide (900 mL) were mixed and the reaction was stirred for 4 hours at room temperature. After completion of the reaction, the reaction mixture was diluted with toluene (1.2 L) and water (1.8 L) and stirring was continued for 30 min. After standing and stratifying, the organic layer was separated and washed twice with 900 mL of water. The organic layer was dried with magnesium sulfate and filtered to remove the desiccant. The filtrate was concentrated and the residue was dried by vacuum pump overnight to give 191.71 g of the target product in 89.9% yield.

References

[1] Patent: US5310928, 1994, A
[2] Patent: US5130439, 1992, A

83857-96-9
589-15-1
143722-29-6
Synthesis of N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde from 2-Butyl-4-chloro-5-formylimidazole and 4-Bromobenzyl bromide

N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde Preparation Products And Raw materials

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1H-Imidazole-5-carboxaldehyde, 1-[(4-bromophenyl)methyl]-2-butyl-4-chloro- N-(4-Bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carboxyaldehyde 1-[(4-BroMophenyl)Methyl]-2-butyl-4-chloro-1H-iMidazole-5-carboxaldehyde 1-(4-bromobenzyl)-2-butyl-4-chloro-1H-imidazole-5-carbaldehyde 3-[(4-Bromophenyl)methyl]-2-butyl-5-chloroimidazole-4-carbaldehyde Butanoicacid,4-chloro-6-oxo- 1-(1H-1,3-BENZODIAZOL-2-YL)-1H-PYRAZOL-7-AMINE 143722-29-6 C15H16BrClN2O Aromatics Heterocycles Intermediates