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Cyclopentyl-(4-chlorophenyl)methanol is an organic compound with the chemical formula C12H15ClO. It is a colorless to pale yellow liquid with a molecular weight of 212.69 g/mol. cyclopentyl-(4-chlorophenyl)methanol is characterized by a cyclopentyl group attached to a benzylic alcohol moiety, with a 4-chlorophenyl substituent. It is synthesized through various chemical reactions and is used as an intermediate in the production of pharmaceuticals and agrochemicals. Due to its potential applications in the synthesis of various compounds, cyclopentyl-(4-chlorophenyl)methanol is of interest in the fields of organic chemistry and medicinal chemistry.

2205-00-7

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2205-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2205-00-7 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 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2205-00:
(6*2)+(5*2)+(4*0)+(3*5)+(2*0)+(1*0)=37
37 % 10 = 7
So 2205-00-7 is a valid CAS Registry Number.

2205-00-7Downstream Products

2205-00-7Relevant academic research and scientific papers

Alkylation of aromatic aldehydes with alkylboron chloride derivatives

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

, p. 1663 - 1670 (2007/10/03)

The reaction of aryl aldehydes with alkylboron chlorides has been investigated. Monoalkylboron dichlorides react with aryl aldehydes in hexane under reflux conditions to give a mixture of dichloroarylmethane and benzyl chloride. Under the same reaction conditions, dialkylboron chlorides lead to formation of a mixture of benzyl chloride and the chloroalkylation product. In the presence of a base such as 2,6-lutidine, the reactions of monoalkylboron dichlorides with aryl aldehydes yield small amounts of the desired alkylation products at room temperature. Dialkylboron chlorides react with aryl aldehydes in hexane in the presence of base to generate the corresponding arylalkylmethanols in good yields.

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