532406-56-7

Basic information

• Product Name: 4-iodo-3-nitrobenzoyl chloride
• Synonyms: 4-iodo-3-nitrobenzoyl chloride
• CAS NO: 532406-56-7
• Molecular Weight: 311.463
• Mol File: 532406-56-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-iodo-3-nitrobenzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-iodo-3-nitrobenzoyl chloride(532406-56-7)
• EPA Substance Registry System: 4-iodo-3-nitrobenzoyl chloride(532406-56-7)

Safety Data

• Hazardous Substances Data: 532406-56-7(Hazardous Substances Data)

Upstream product

• 27329-27-7 4-methyl-2-nitrobenzoic acid 
• 5326-39-6 4-iodo-3-nitrotoluene 
• 1588-83-6 4-amino-3-nitrobenzoic acid 
• 35674-27-2 4-iodo-3-nitrobenzoic acid 

Downstream Products

• 17319-37-8 O-(4-iodo-3-nitro-benzoyloxy)-ergocalciferol 
• 875271-83-3 [5-(4-iodo-3-nitro-benzoyl)-2-phenyl-thiophen-3-yl]-acetic acid methyl ester 
• 875271-84-4 [5-(3-amino-4-iodo-benzoyl)-2-phenyl-thiophen-3-yl]-acetic acid methyl ester 
• 875271-81-1 [5-(4-iodo-3-nitrobenzoyl)-2-phenylthiophen-3-yl]acetic acid 
• 1021171-80-1 [5-(3-tert-butoxycarbonylamino-4-iodo-benzoyl)-2-phenyl-thiophen-3-yl]-acetic acid methyl ester 
• 875271-82-2 (5-{3-[(tert-butoxycarbonyl)amino]-4-iodobenzoyl}-2-phenylthiophene-3-yl)acetic acid 
• 1004752-86-6 methyl 2-(2-bromo-5-(4-iodo-3-nitrobenzoyl)thiophen-3-yl)acetate 
• 1374326-50-7 Ethyl 2-(2-bromo-5-(4-iodo-3-nitrobenzoyl)thiophen-3-yl)acetate 
• 1374035-40-1 N-methyl-4-(2-(trimethylsilyl)ethynyl)-3-nitrobenzamide 
• 1374035-16-1 N-methyl-4-ethynyl-3-nitrobenzamide 
• 1374035-34-3 N-methyl-4-cyano-3-nitrobenzamide 
• 1374035-39-8 N-methyl-4-iodo-3-nitrobenzamide 
• 160003-66-7 4-iodo-3-nitrobenzamide 

Relevant articles and documents

Inexpensive NaX (X = I, Br, Cl) as a halogen donor in the practical Ag/Cu-mediated decarboxylative halogenation of aryl carboxylic acids under aerobic conditions

Versatile and practical Ag/Cu-mediated decarboxylative halogenation between readily available aryl carboxylic acids and abundant NaX (X = I, Br, Cl) has been achieved under aerobic conditions in moderate to good yields. The halodecarboxylation is shown to be an effective strategy for S-containing heteroaromatic carboxylic acid and benzoic acids with nitro, chloro and methoxyl substituents at the ortho position. A gram-scale reaction and a three-step procedure to synthesize iniparib have been performed to evaluate the practicality of this protocol. A preliminary mechanistic investigation indicates that Cu plays a vital role and a radical pathway is involved in the transformation.

The flocculated acryloyldimethyltauric molecule ligand

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SMALL-MOLECULE BOTULINUM TOXIN INHIBITORS

Small-molecule inhibitors of Botulinum toxin, including BoNTA, BoNTD and BoNTE are provided, as well as methods of using the inhibitors.