4153-07-5

Basic information

• Product Name: 2-nitro-4-methoxylbenzenesulphenyl chloride
• CAS NO: 4153-07-5
• Molecular Weight: 219.649
• Mol File: 4153-07-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-nitro-4-methoxylbenzenesulphenyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-nitro-4-methoxylbenzenesulphenyl chloride(4153-07-5)
• EPA Substance Registry System: 2-nitro-4-methoxylbenzenesulphenyl chloride(4153-07-5)

Safety Data

• Hazardous Substances Data: 4153-07-5(Hazardous Substances Data)

Upstream product

• 14371-84-7 4,4′-dimethoxy-2,2′-dinitro-diphenyl disulfide 
• 10298-80-3 2-chloro-5-methoxynitrobenzene 
• 5344-78-5 4-bromo-3-nitroanizole 
• 96-96-8 4-methoxy-2-nitroaniline 

Downstream Products

• 17191-20-7 2-Nitro-4-methoxyphenylsulfenyl-DL-C-phenylglycin 
• 17191-18-3 2-Nitro-4-methoxyphenylsulfenylglycin 
• 17191-26-3 2-Nitro-4-methoxyphenylsulfenyl-L-valin 
• 17191-22-9 2-Nitro-4-methoxyphenylsulfenyl-L-alanin 
• 71339-62-3 C₂₂H₂₀N₂O₃S 
• 72444-14-5 methyl (2SR,10RS)-2-<(4-methoxy-2-nitrophenyl)thio>-4-oxatricyclo<4.3.1.0^3,7>deca-5-one-10-carboxylate 
• 72444-09-8 methyl (2SR,7RS)-2-<(4-methoxy-2-nitrophenyl)thio>-4-oxa-5-oxotricyclo<4.4.0.0^3,8>decane-7-carboxylate 
• 74880-35-6 (1S,2S,3R,4R,6R)-1-(1-Chloro-ethyl)-3-(4-methoxy-2-nitro-phenylsulfanyl)-tricyclo[2.2.1.0^2,6]heptane 
• 74880-24-3 (1S,2S,3R,4R,6R)-1-Chloromethyl-3-(4-methoxy-2-nitro-phenylsulfanyl)-tricyclo[2.2.1.0^2,6]heptane 

Relevant articles and documents

Electrophilic cleavage of cyclopropanes. II. Concerning the effect of increasing electron demand upon the product-determining transition state in the reaction of 4-substituted-2-nitrobenzenesulphenyl chlorides and benzenesulphenyl chlorides with tetracyclo2,7.04,6>heptane....

The effect of increasing electron demand upon the product-determining transition state in the reaction of arenesulphenyl chlorides with tetracyclo2,7.04,6>heptane has been investigated.As the electron donating ability of the remote substituents on the phenyl ring of the sulphenyl chloride is varied from nitro to methoxy the relative proportion of adducts derived from edge-on attack is found to increase relative to that of adducts derived from corner attack.An ortho-nitro group was found to lead to a stabilizing interaction only in the case of 2,4-dinitrobenzenesulphenyl chloride.A mechanism involving the competition between the two conceptual modes of approach is suggested.