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Benzenemethanol, 3-bromo-α-methyl-α-phenyl-, also known as 3-bromo-α-methylbenzeneethanol or 3-bromo-α-methylphenethyl alcohol, is an organic compound with the chemical formula C14H15BrO. It is a derivative of benzyl alcohol, featuring a bromine atom at the 3-position, an α-methyl group, and a phenyl ring. Benzenemethanol, 3-bromo-a-methyl-a-phenyl- is characterized by its unique structure, which combines the properties of benzyl alcohol with the presence of a bromine atom and an additional methyl group. It is used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and chemical industries, due to its versatile functional groups and potential for further modification.

90862-33-2

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90862-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90862-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,8,6 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90862-33:
(7*9)+(6*0)+(5*8)+(4*6)+(3*2)+(2*3)+(1*3)=142
142 % 10 = 2
So 90862-33-2 is a valid CAS Registry Number.

90862-33-2Relevant academic research and scientific papers

Preparation and morphology of ring-shaped polystyrene-block-polyisoprenes

Takano, Atsushi,Kadoi, Osamu,Hirahara, Kazuhiro,Kawahara, Seiichi,Isono, Yoshinobu,Suzuki, Jiro,Matsushita, Yushu

, p. 3045 - 3050 (2007/10/03)

Three polystyrene-block-polyisoprene-block-polystyrenes (SIS) with different compositions were prepared and cyclized by the coupling reaction between two end groups on the same molecules. Ring-shaped polystyrene-block-polyisoprenes (SI) were isolated from

Highly asymmetric dihydroxylation of 1-aryl-1'-pyridyl alkenes

Wang, Xin,Zak, Mark,Maddess, Mathew,O'Shea, Paul,Tillyer, Richard,Grabowski,Reider, Paul J.

, p. 4865 - 4869 (2007/10/03)

The asymmetric dihydroxylation of 1-aryl-1'-pyridyl alkenes afforded the diols in high yield and excellent enantioselectivity. (C) 2000 Published by Elsevier Science Ltd.

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