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Benzenemethanol, 2-(methylsulfinyl)-, also known as 2-(methylsulfinyl)benzenemethanol or alpha-methylsulfinylbenzyl alcohol, is an organic compound with the chemical formula C8H10OS. It is a colorless to pale yellow liquid with a molecular weight of 154.23 g/mol. Benzenemethanol, 2-(methylsulfinyl)- is characterized by the presence of a benzene ring with a hydroxyl group (-OH) attached to the 2-position and a methylsulfinyl group (-S(O)CH3) at the same position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can undergo further chemical reactions, such as oxidation, reduction, and substitution, making it a valuable building block in organic chemistry.

62351-52-4

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62351-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62351-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,5 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62351-52:
(7*6)+(6*2)+(5*3)+(4*5)+(3*1)+(2*5)+(1*2)=104
104 % 10 = 4
So 62351-52-4 is a valid CAS Registry Number.

62351-52-4Downstream Products

62351-52-4Relevant academic research and scientific papers

NEIGHBOURING-GROUP PARTICIPATION IN THE OXIDATION OF SULPHIDES WITH HYDROGEN PEROXIDE

Ruff, Ferenc,Kucsman, Arpad

, p. 241 - 246 (2007/10/02)

Using a set of sulphides (o- and p-XC6H4SMe), the electronic effect, steric hindrance and anchimeric assistance for the O-transfer by H2O2 have been investigated by a kinetic method.The steric effect and anchimeric assistance were evaluated by comparing t

Electronic effect, steric hindrance, and anchimeric assistance in oxidation of sulphides. Neighbouring-group participation through Sulphur-oxygen nonbonded interaction

Ruff, Ferenc,Kucsman, Arpad

, p. 1123 - 1128 (2007/10/02)

Using a set of sulphides o- and p-XC6H4SMe, the electronic effect, steric hindrance, and anchimeric assistance for electrophilic Cl+ addition by TsNHCI and O-transfer by NalO4 were investigated by a kinetic method. The steric effect and anchimeric assistance of the ortho-substituents were evaluated by comparing the reactivity of ortho- and para-substituted compounds (K = ko/kp). For neighbouringgroup activity the following order was obtained: CH2OH ~ CH2OMe ~ CH2CO2Me CH2CO2H ~ CH2NMe2 CH2C02 - ~ CHO CO2Me ~ CO2H COMe ~ CONH2 C02- Reaction rates show that the anchimeric assistance is governed by an S mellip; 0 or S ... N close contact developed in the transition state between oppositely polarized heteroatoms. Factors controlling neighbouringgroup participation through attractive non-bonded interactions are discussed.

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