91760-66-6

Basic information

• Product Name: 3-BroMo-4-forMylbenzoic acid
• Synonyms: 3-BroMo-4-forMylbenzoic acid;2-BroMo-4-forMylbenzoic acid
• CAS NO: 91760-66-6
• Molecular Formula: C₈H₅BrO₃
• Molecular Weight: 229.0275
• Mol File: 91760-66-6.mol
• Article Data: 9

Chemical Properties

• Melting Point: 239℃ (N,N-dimethylformamide hexane ethyl acetate )
• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 3-BroMo-4-forMylbenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BroMo-4-forMylbenzoic acid(91760-66-6)
• EPA Substance Registry System: 3-BroMo-4-forMylbenzoic acid(91760-66-6)

Safety Data

• Hazardous Substances Data: 91760-66-6(Hazardous Substances Data)

Usage

General Description

3-Bromo-4-formylbenzoic acid, also known as 3-bromo-4-carboxaldehydebenzoic acid, is a chemical compound with the molecular formula C8H5BrO3. It is a derivative of benzoic acid and is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. 3-BroMo-4-forMylbenzoic acid is also used in the production of dyes and pigments. It is a white to light yellow solid that is soluble in organic solvents such as methanol and dichloromethane. 3-Bromo-4-formylbenzoic acid is a versatile building block in organic synthesis and has applications in various industries.

Upstream product

• 1001200-40-3 methyl 3-bromo-4-(dibromomethyl)benzoate 
• 90001-43-7 2-bromobenzene-1,4-dicarbaldehyde 
• 7697-26-9 3-bromo-4-methylbenzoic acid 
• 42872-74-2 3-bromo-4-methyl-benzonitrile 
• 89891-69-0 3-bromo-4-formyl benzonitrile 
• 89892-39-7 3-bromo-4-(bromomethyl)benzonitrile 
• 90004-92-5 3-Brom-terephthalaldehydamid 

Downstream Products

• 90221-60-6 2-Brom-4-hydroxymethyl-benzoesaeure 
• 1331832-73-5 C₂₄H₂₇BrO₂ 
• 1403326-73-7 2-bromo-4-(1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)carbonyl)benzoic acid 
• 1403326-82-8 4-((benzyloxy)carbonyl)-2-bromobenzoic acid 
• 1403326-85-1 4-benzyl 1-methyl 2-bromobenzene-1,4-dioate 
• 264272-63-1 2-bromo-1,4-benzenedicarboxylic acid,1-methyl ester 
• 1204305-02-1 methyl 2-bromo-4-(chloro-carbonyl)-benzoate 
• 1403326-89-5 methyl 2-bromo-4-(1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)carbonyl)benzoate 
• 1403326-69-1 methyl 2-bromo-4-(1-(1,2,3,4-tetrahydro-1,1,4,4,6-pentamethylnaphthalen-7-yl)vinyl)benzoate 
• 1403326-79-3 benzyl-3-bromo-4-formylbenzoate 
• 1613621-87-6 (S)-4-(2-bromo-4-carboxyphenyl)-6-methyl-2-thioxo-1-(3-trifluoromethylphenyl)-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid methyl ester (+)-cinchonine salt 

Relevant articles and documents

Oxidation of aromatic and aliphatic aldehydes to carboxylic acids by Geotrichum candidum aldehyde dehydrogenase

Oxidation reaction is one of the most important and indispensable organic reactions, so that green and sustainable catalysts for oxidation are necessary to be developed. Herein, biocatalytic oxidation of aldehydes was investigated, resulted in the synthesis of both aromatic and aliphatic carboxylic acids using a Geotrichum candidum aldehyde dehydrogenase (GcALDH). Moreover, selective oxidation of dialdehydes to aldehydic acids by GcALDH was also successful.

TETRAHYDROTRIAZOLOPYRIMIDINE DERIVATIVES AS HUMAN NEUTROPHIL ELASTASE INHIBITORS

This invention relates to heterocyclic compounds, which are pyrimidinone derivatives having human neutrophil elastase inhibitory properties, and their use in therapy.

NOVEL COMPOUNDS

Compounds of formula (I), described herein, exhibit human neutrophil elastase inhibitory properties, and are useful for the treatment of diseases and conditions in which HNE is implicated.