7305-07-9

Basic information

• Product Name: Carbamic acid, dimethyl-, 3-methylphenyl ester
• CAS NO: 7305-07-9
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.219
• Mol File: 7305-07-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Carbamic acid, dimethyl-, 3-methylphenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, dimethyl-, 3-methylphenyl ester(7305-07-9)
• EPA Substance Registry System: Carbamic acid, dimethyl-, 3-methylphenyl ester(7305-07-9)

Safety Data

• Hazardous Substances Data: 7305-07-9(Hazardous Substances Data)

Upstream product

• 506-59-2 N,N-dimethylammonium chloride 
• 1885-14-9 phenyl chloroformate 
• 108-39-4 3-methyl-phenol 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 

Downstream Products

• 1375931-48-8 2-bromo-5-methylphenyl dimethylcarbamate 
• 1341217-46-6 (E)-ethyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-4-methylphenyl}acrylate 
• 1414838-27-9 (E)-methyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-4-methylphenyl}acrylate 
• 1414838-28-0 (E)-benzyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-4-methylphenyl}acrylate 
• 50715-82-7 3-methyl-5-phenyl-phenol 
• 1445899-06-8 2-hydroxy-5-methylphenyl dimethylcarbamate 
• 1309752-04-2 (E)-n-butyl 3-{2-[(N,N-dimethylcarbamoyl)oxy]-4-methylphenyl}acrylate 
• 29285-52-7 2-chloro-5-methylphenyl dimethylcarbamate 

Relevant articles and documents

Synthesizing method of multi-aryl substituted naphthol derivate

The invention discloses a synthesizing method of a multi-aryl substituted naphthol derivate. The method comprises the following steps: performing cyclization reaction on a phenol derivate and a diaromatic acetylene derivate in an organic solvent under the

Room-temperature Pd-catalyzed C-H chlorination by weak coordination: One-pot synthesis of 2-chlorophenols with excellent regioselectivity

A room-temperature Pd(ii)-catalyzed regioselective chlorination reaction has been developed for a facile one-pot synthesis of a broad range of 2-chlorophenols. The reaction demonstrates an excellent regioselectivity and reactivity for C-H chlorination. This reaction represents one of the rare examples of mild C-H functionalization at ambient temperature.

High-yielding, versatile, and practical [Rh(III)Cp*]-catalyzed ortho bromination and iodination of arenes

We report a uniquely high-yielding, general, and practical ortho bromination and iodination reaction of different classes of aromatic compounds. This reaction occurs by Rh(III)-catalyzed C-H bond activation methodology and is therefore the first example of the application of this cationic catalyst for C-Br and C-I bond formation.