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(p-Bromophenyl)-cyclopentyl-methanol is a complex organic compound characterized by a cyclopentyl group attached to a methanol molecule, with a p-bromophenyl group as a substituent. (p-bromophenyl)-cyclopentyl-methanol is composed of a cyclopentane ring, a hydroxyl group, and a bromine atom attached to a benzene ring. The presence of the bromine atom and the cyclopentyl group contributes to its unique chemical properties, making it a potentially useful intermediate in the synthesis of various pharmaceuticals and other organic compounds. Its molecular formula is C12H17BrO, and it exhibits a molecular weight of 249.17 g/mol. Due to its specific structure, (p-bromophenyl)-cyclopentyl-methanol may have applications in the development of new drugs, agrochemicals, or other specialty chemicals, although further research and testing would be required to determine its specific uses and safety profile.

2204-99-1

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2204-99-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2204-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2204-99:
(6*2)+(5*2)+(4*0)+(3*4)+(2*9)+(1*9)=61
61 % 10 = 1
So 2204-99-1 is a valid CAS Registry Number.

2204-99-1Downstream Products

2204-99-1Relevant academic research and scientific papers

Indium-copper and indium-silver mediated Barbier-Grignard-type alkylation reaction of aldehydes using unactivated alkyl halides in water

Shen, Zhi-Liang,Yeo, Yan-Lin,Loh, Teck-Peng

, p. 3922 - 3924 (2008/09/19)

(Chemical Equation Presented) An efficient method has been developed for the Barbier-Grignard-type alkylation reaction of aldehydes (including aliphatic version) using unactivated alkyl halides in water in the presence of an In/CuI/I2 or In/AgI/I2 system. The reactions proceeded more efficiently in water than in organic solvent. In, CuI or AgI, and I 2 were all essential for the efficient progress of the reactions. A radical-type reaction mechanism was studied and proposed by using 4-pentenal as substrate.

A new method for alkylation of aromatic aldehydes using alkylboron chloride derivatives in the presence of oxygen

Kabalka, George W,Wu, Zhongzhi,Ju, Yuhong

, p. 3243 - 3248 (2007/10/03)

Reactions of aromatic aldehydes with alkylboron chloride derivatives in the presence of oxygen have been investigated. Dialkylboron chlorides react with aryl aldehydes to produce arylalkylmethanols in good to excellent yields. Under the same reaction conditions, alkylboron dichlorides lead to the formation of arylalkyl chlorides.

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