246511-70-6

Basic information

• Product Name: 1-bromo-2-methyl-4-(4-nitrophenoxy)benzene
• CAS NO: 246511-70-6
• Molecular Weight: 308.131
• Mol File: 246511-70-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-bromo-2-methyl-4-(4-nitrophenoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-2-methyl-4-(4-nitrophenoxy)benzene(246511-70-6)
• EPA Substance Registry System: 1-bromo-2-methyl-4-(4-nitrophenoxy)benzene(246511-70-6)

Safety Data

• Hazardous Substances Data: 246511-70-6(Hazardous Substances Data)

Upstream product

• 2303-25-5 3-methyl-4'-nitrodiphenyl ether 
• 100-00-5 4-chlorobenzonitrile 
• 108-39-4 3-methyl-phenol 

Downstream Products

• 873977-84-5 acetic acid-[4-(4-bromo-3-methyl-phenoxy)-2-nitro-anilide] 
• 873980-25-7 4-(4-bromo-3-methyl-phenoxy)-2-nitro-aniline 
• 860597-21-3 2-bromo-5-(4-nitro-phenoxy)-benzoic acid 
• 873977-88-9 acetic acid-[4-(4-bromo-3-methyl-phenoxy)-anilide] 

Relevant articles and documents

COMPOUNDS FOR THE TREATMENT OF ONCOVIRUS INDUCED CANCER AND METHODS OF USE THEREOF

The pesent invention relates to compounds of formula (I) pharmaceutically-acceptable salts, hydrates, solvates, or stereoisomers thereof and their use for the prevention and treatment of oncovirus induced cancer in a subject.

Synthesis of substituted benzyl 2-methyl-2-phenylpropyl ethers and their moth-proofing activity on wool against larvae of Anthrenus fasciatus

Synthesis of new moth-proofing agents is necessary to overcome the damage caused by clothes moths and carpet beetles to hosiery and upholstery. In the present paper substituted benzyl 2-methyl-2-phenylpropyl ethers were synthesised and evaluated for moth-proofing activity. Two compounds were found to provide protection against larvae of Anthrenus fasciatus at levels of 1.0 and 10 g kg-1 respectively. The introduction of a methyl group in the para position of the benzene ring attached to C2 of the 2-methylpropyl chain (ring A) increased moth-proofing activity. The introduction of a phenoxy ring at the meta position of the benzyl nucleus (ring B) also increased activity, while the presence of a nitro group on the benzyl nucleus (ring B) decreased activity.