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3-bromophenyl dimethylcarbamate is an organic compound with the chemical formula C9H10BrNO2. It is a derivative of phenol, where one of the hydrogen atoms on the benzene ring is replaced by a bromine atom, and the hydroxyl group is converted into a carbamate group. 3-bromophenyl dimethylcarbamate is characterized by its potential use as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, due to its ability to form stable derivatives and participate in a range of chemical reactions. It is also known for its potential applications in the development of new materials and as a reagent in organic synthesis. The compound's properties, such as its reactivity and stability, make it a valuable component in the creation of more complex molecules.

7305-05-7

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7305-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7305-05-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7305-05:
(6*7)+(5*3)+(4*0)+(3*5)+(2*0)+(1*5)=77
77 % 10 = 7
So 7305-05-7 is a valid CAS Registry Number.

7305-05-7Relevant academic research and scientific papers

Rhodium-catalyzed selective C-H activation/olefination of phenol carbamates

Gong, Tian-Jun,Xiao, Bin,Liu, Zhao-Jing,Wan, Jian,Xu, Jun,Luo, Dong-Fen,Fu, Yao,Liu, Lei

, p. 3235 - 3237 (2011)

Rh(III)-catalyzed ortho C-H activation/olefination of phenol carbamates has been developed. High regioselectivity is observed with a range of phenol carbamates enabling efficient coupling with acrylates and styrenes. This reaction exhibits different react

Synthesizing method of multi-aryl substituted naphthol derivate

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Paragraph 0058; 0059; 0060; 0061, (2017/12/27)

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

Pd(II) catalyzed ortho C-H iodination of phenylcarbamates at room temperature using cyclic hypervalent iodine reagents

Sun, Xiuyun,Yao, Xia,Zhang, Chao,Rao, Yu

supporting information, p. 10014 - 10017 (2015/06/22)

A novel approach to access ortho iodinated phenols using cyclic hypervalent iodine reagents through palladium(II) catalyzed C-H activation has been developed through weak coordination. The reaction showed excellent regioselectivity, reactivity and good functional group tolerance. A unique mechanism was proposed.

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

Sun, Xiuyun,Sun, Yonghui,Zhang, Chao,Rao, Yu

supporting information, p. 1262 - 1264 (2014/02/14)

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.

A general approach towards catechol and pyrogallol through ruthenium- and palladium-catalyzed C-H hydroxylation by weak coordination

Yang, Xinglin,Sun, Yonghui,Chen, Zhang,Rao, Yu

supporting information, p. 1625 - 1630 (2014/06/09)

An efficient ruthenium(II)- and palladium(II)-catalyzed C-H hydroxylation of aryl carbamates has been developed for the facile synthesis of catechols and pyrogallols. The reaction demonstrates excellent reactivity, regio- and chemoselectivity, good functional group compatibility and high yields. The practicality of this method has been proved by a gram-scale synthesis.

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