42747-54-6

Basic information

• Product Name: Benzoyl chloride, 2-chloro-3,5-dinitro-
• CAS NO: 42747-54-6
• Molecular Formula: C7H2Cl2N2O5
• Molecular Weight: 265.009
• Mol File: 42747-54-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 2-chloro-3,5-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-chloro-3,5-dinitro-(42747-54-6)
• EPA Substance Registry System: Benzoyl chloride, 2-chloro-3,5-dinitro-(42747-54-6)

Safety Data

• Hazardous Substances Data: 42747-54-6(Hazardous Substances Data)

Upstream product

• 10026-13-8 phosphorus pentachloride 
• 2497-91-8 2-chloro-3,5-dinitrobenzoic acid 
• 69-72-7 salicylic acid 
• 609-99-4 3,5-dinitrosalicylic acid 

Downstream Products

• 2213-79-8 methyl 2-chloro-3,5-dinitrobenzoate 
• 42747-56-8 2-chloro-3,5-dinitro-benzoic acid anilide 
• 854024-30-9 2-chloro-4'-methyl-3,5-dinitro-benzophenone 
• 92074-93-6 N-(2-Chlor-3,5-dinitrobenzoyl)-S,S-dimethylschwefeldiimid 
• 177035-49-3 2-chloro-N-(2,3-dihydroxypropyl)-3,5-dinitrobenzamide 
• 27697-45-6 2-chloro-3,5-dinitrobenzonitrile 
• 22603-53-8 1-amino-2-cyano-4,6-dinitrobenzene 
• 24170-60-3 3-acetylamino-4-(2'-cyano-4',6'-dinitrophenylazo)-N,N-diethylaniline 
• 83907-91-9 2-(4-Methyl-1-piperazinyl)-3,5-dinitro-N-(4-nitrophenyl)benzamide 
• 680199-29-5 2-chloro-3,5-dinitro-N-(2-hydroxyethyl)benzamide 
• 6266-51-9 2-chloro-3,5-dinitrobenzamide 
• 1352562-36-7 6,8-dinitro-2-(4-(trifluoromethyl)anilino)-4H-benzo[e][1,3]thiazine-4-thione 
• 1449698-47-8 C₈H₂ClN₃O₅S 
• 680199-38-6 3-[(2-chloro-3,5-dinitrobenzoyl)amino]propanoate 

Relevant articles and documents

Synthesis and structure-activity relationships evaluation of benzothiazinone derivatives as potential anti-tubercular agents

N-Alkyl and heterocycle substituted 1,3-benzothiazin-4-one (BTZ) derivatives were synthesized. The anti-mycobacterial activities of these compounds were evaluated by determination of minimal inhibitory concentration (MIC) for Mycobacterium tuberculosis H3

NITROANILINE-BASED ALKYLATING AGENTS AND THEIR USE AS PRODRUGS

Nitroaniline-based unsymmetrical mustards of the general formula (I) are provided, together with methods of preparation and methods for their use as produgs for gene-dependent enzyme prodrug therapy (GDEPT) and cell ablation therapy in conjuction with nit

Hypoxia-selective antitumor agents. 14. Synthesis and hypoxic cell cytotoxicity of regioisomers of the hypoxia-selective cytotoxin 5-[N,N- bis(2-chloroethyl)amino]-2,4-dinitrobenzamide

A series of regioisomers of the novel hypoxia-selective cytotoxin (HSC) 5- [N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamide (2a) have been prepared by displacement of the chloro group from methyl chlorodinitrobenzoates or the corresponding carboxamides