22812-61-9

Basic information

• Product Name: Benzoic acid, 3,5-dibromo-4-methoxy-, methyl ester
• CAS NO: 22812-61-9
• Molecular Formula: C9H8Br2O3
• Molecular Weight: 323.969
• Mol File: 22812-61-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3,5-dibromo-4-methoxy-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3,5-dibromo-4-methoxy-, methyl ester(22812-61-9)
• EPA Substance Registry System: Benzoic acid, 3,5-dibromo-4-methoxy-, methyl ester(22812-61-9)

Safety Data

• Hazardous Substances Data: 22812-61-9(Hazardous Substances Data)

Upstream product

• 3337-62-0 3,5-dibromo-4-hydroxybenzoic acid 
• 41727-47-3 methyl 3,5-dibromo-4-hydroxybenzoate 
• 74-88-4 methyl iodide 
• 121-98-2 methyl 4-methoxybenzoate 

Downstream Products

• 340216-49-1 3,5-dibromo-4-methoxybenzohydrazide 
• 1422570-19-1 3-(5-(3,5-dibromo-4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)benzene-1-sulfonyl fluoride 
• 1422570-82-8 4-(5-(3,5-dibromo-4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)benzene-1-sulfonyl fluoride 
• 1422570-01-1 3-(5-(3,5-dibromo-4-hydroxyphenyl)-1,3,4-oxadiazol-2-yl)benzene-1-sulfonyl fluoride 
• 1422570-37-3 4-(5-(3,5-dibromo-4-hydroxyphenyl)-1,3,4-oxadiazol-2-yl)benzene-1-sulfonyl fluoride 
• 4073-36-3 3,5-dibromo-4-methoxybenzoyl chloride 
• 4073-35-2 3,5-dibromo-4-methoxybenzoic acid 

Relevant articles and documents

Chemical Identity and Mechanism of Action and Formation of a Cell Growth Inhibitory Compound from Polycarbonate Flasks

This paper reports the chemical identity and mechanism of action and formation of a cell growth inhibitory compound leached from some single-use Erlenmeyer polycarbonate shaker flasks under routine cell culture conditions. Single-use cell culture vessels

A convenient and efficient H2SO4-promoted regioselective monobromination of phenol derivatives using N-bromosuccinimide

A convenient, rapid H2SO4-promoted regioselective monobromination reaction with N-bromosuccinimide was developed. The desired para-monobrominated or ortho-monobrominated products of phenol derivatives were obtained in good to excellent yields with high selectivity. Regioselective chlorination and iodination were also achieved in the presence of H2SO4 using N-chlorosuccinimide and N-iodosuccinimide, respectively.

N-HYDROXYAMIDE DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

Novel N-hydroxyamide derivatives are disclosed. These N-hydroxyamide derivatives inhibit UPD-3O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase, an enzyme present in gram negative bacteria and are therefore useful as antimicrobials and antibiotics. Methods of synthesis and of use of the compounds are also disclosed.