13277-61-7

Basic information

• Product Name: Benzoyl bromide, 4-nitro-
• Synonyms: Benzoyl bromide,4-nitro;4-nitro-benzoyl bromide;4-Nitro-benzoylbromid;p-Nitrobenzoyl bromide
• CAS NO: 13277-61-7
• Molecular Formula: C7H4BrNO3
• Molecular Weight: 230.018
• Mol File: 13277-61-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoyl bromide, 4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl bromide, 4-nitro-(13277-61-7)
• EPA Substance Registry System: Benzoyl bromide, 4-nitro-(13277-61-7)

Safety Data

• Hazardous Substances Data: 13277-61-7(Hazardous Substances Data)

Upstream product

• 62-23-7 4-nitro-benzoic acid 
• 555-16-8 4-nitrobenzaldehdye 
• 521281-91-4 C₇H₄BrNO₂ 
• 15219-34-8 Oxalyl bromide 
• 122-04-3 4-nitro-benzoyl chloride 

Downstream Products

• 619-50-1 4-nitrobenzoic acid methyl ester 
• 6388-74-5 p-Nitrophenyloxirane 
• 6749-93-5 cyclopropylmethyl p-nitrobenzoate 
• 99-78-5 isobutyl p-nitrobenzoate 
• 15727-80-7 allyl 4-nitrobenzoate 
• 14786-27-7 benzyl 4-nitrobenzoate 
• 22956-96-3 4-nitro-benzoic acid-(2-methoxy-4-propyl-phenyl ester) 
• 108791-66-8 1,4‐bis(4‐nitrophenyl)butane‐1,4‐dione 
• 5323-47-7 N,N-diethyl-4-nitrobenzamide 
• 2585-24-2 N-n-propyl-4-nitrobenzamide 
• 51207-98-8 N-butyl-4-nitrobenzamide 
• 14309-42-3 pentyl 4-nitrobenzoate 
• 803733-46-2 tri-O-benzoyl-O-(4-nitrobenzyl)pentaerythritol 
• 325856-42-6 rac-2-azido-2-(para-nitro-phenyl)-ethanol 

Relevant articles and documents

Synthesis and Anti-Oomycete Activity of 1-Sulfonyloxy/Acyloxydihydroeugenol Derivatives

Endeavor to discover biorational natural products-based fungicides, two series (26) of novel 1-sulfonyloxy/acyloxydihydroeugenol derivatives (3a–p and 5a–j) were prepared and assessed for their fungicidal activity against P. capsici Leonian, in vitro. Res

Convenient metal-free direct oxidative amidation of aldehyde using dibromoisocyanuric acid under mild conditions

A facile method for the direct synthesis of amides from aldehydes is described. Amide bonds were synthesized by an oxidative amidation in the presence of dibromoisocyanuric acid (DBI). Treatment of aromatic and aliphatic aldehydes with dibromoisocyanuric acid generated acyl bromide intermediates, which were employed to react with a variety of secondary and primary amines to give amides. Through this reaction method, various amides were synthesized directly from aldehydes under mild conditions in high yields and short times. This facile and efficient procedure provides potential strategy for the direct synthesis of amides from aldehydes.

A mild and efficient reaction for conversion of carboxylic acids into acid bromides with ethyl tribromoacetate/triphenylphosphine under acid-free conditions

Acid bromides were prepared efficiently from carboxylic acids with readily available ethyl tribromoacetate and triphenylphosphine at room temperature under neutral conditions. The present process is applicable to the preparation of various acid bromides from aromatic and aliphatic carboxylic acids. Aromatic carboxylic acids were found to be more reactive than aliphatic carboxylic acids under reaction conditions.