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α-(p-Cyclopropylphenyl)ethanol, also known as 1-(4-cyclopropylphenyl)ethanol, is an organic compound with the chemical formula C11H14O. It is a colorless liquid with a molecular weight of 162.23 g/mol. α-(p-Cyclopropylphenyl)aethanol is characterized by a cyclopropyl group attached to a phenyl ring, with an ethanol group (-CH2CH2OH) at the alpha position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antidepressants and insecticides. Due to its potential applications in the development of therapeutic agents, α-(p-Cyclopropylphenyl)ethanol is of interest in the fields of medicinal chemistry and chemical research.

40641-97-2

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40641-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40641-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,4 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40641-97:
(7*4)+(6*0)+(5*6)+(4*4)+(3*1)+(2*9)+(1*7)=102
102 % 10 = 2
So 40641-97-2 is a valid CAS Registry Number.

40641-97-2Relevant academic research and scientific papers

Direct synthesis of ethers from aldehydes and ketones. One-pot reductive etherification of benzaldehydes, alkyl aryl ketones, and benzophenones

Mochalov,Fedotov,Trofimova,Zefirov

, p. 503 - 512 (2016/06/13)

Benzyl alcohols formed by the reduction of benzaldehydes, alkyl aryl ketones, and benzophenones with sodium tetrahydridoborate in alcohols undergo in situ etherification with the solvent in the presence of a catalytic amount of HCl. Thus the process may be regarded as one-pot transformation of carbonyl compounds into the corresponding benzyl ethers. The yields of ethers depend on the substituent nature in the aromatic fragment of the initial carbonyl compound and on the alcohol used as reduction medium.

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