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Benzenemethanol, α-(4-phenyl-1,3-butadienyl)-, also known as 4-phenyl-1,3-butadienylbenzenemethanol or 4-phenyl-1,3-butadienylbenzyl alcohol, is an organic compound with the chemical formula C15H14O. It is a derivative of benzyl alcohol, featuring a phenyl group attached to a 1,3-butadienyl side chain. This molecule is characterized by its aromatic ring structure and a reactive double bond within the butadienyl group, which can participate in various chemical reactions, such as addition and substitution. It is used in the synthesis of pharmaceuticals, fragrances, and other organic compounds due to its unique structure and reactivity.

3185-57-7

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3185-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3185-57-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,8 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3185-57:
(6*3)+(5*1)+(4*8)+(3*5)+(2*5)+(1*7)=87
87 % 10 = 7
So 3185-57-7 is a valid CAS Registry Number.

3185-57-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-diphenylpenta-2,4-dien-1-ol

1.2 Other means of identification

Product number -
Other names 1.5-Diphenylpenta-1.3-dien-1-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3185-57-7 SDS

3185-57-7Relevant academic research and scientific papers

Lithium amidoborane, a highly chemoselective reagent for the reduction of α,β-unsaturated ketones to allylic alcohols

Xu, Weiliang,Zhou, Yonggui,Wang, Ruimin,Wu, Guotao,Chen, Ping

experimental part, p. 367 - 371 (2012/01/13)

Lithium amidoborane (LiNH2BH3, LiAB for short), is capable of chemoselectively reducing α,β-unsaturated ketones to the corresponding allylic alcohols at ambient temperature. A mechanistic study shows that the reduction is via a double hydrogen transfer process. The protic H(N) and hydridic H(B) in amidoborane add to the O and C sites of the carbonyl group, respectively.

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