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Benzenemethanol, α-pentadecyl-, also known as 1-phenylethanol, α-pentadecyl-, is an organic compound with the chemical formula C21H38O. It is a derivative of benzyl alcohol, where a linear pentadecyl (C15H31) alkyl chain is attached to the α-carbon of the benzyl group. Benzenemethanol, a-pentadecyl- is characterized by its long hydrocarbon chain and aromatic ring, which contribute to its unique chemical and physical properties. It is a colorless to pale yellow liquid with a mild, floral odor and is insoluble in water but soluble in organic solvents. Benzenemethanol, α-pentadecyl-, has potential applications in the fragrance and flavor industries due to its pleasant scent and can also be used as a chemical intermediate in the synthesis of various pharmaceuticals and specialty chemicals.

1851-97-4

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1851-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1851-97-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1851-97:
(6*1)+(5*8)+(4*5)+(3*1)+(2*9)+(1*7)=94
94 % 10 = 4
So 1851-97-4 is a valid CAS Registry Number.

1851-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenyl-1-hexadecanol

1.2 Other means of identification

Product number -
Other names Phenylpentadecylcarbinol

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:1851-97-4 SDS

1851-97-4Relevant academic research and scientific papers

Synthesis of new (R)-secondary carbinols with different structures via enzymatic resolution

Yildiz, Tuelay,Yusufolu, Aye

experimental part, p. 1347 - 1352 (2011/11/29)

The present study deals with the biocatalytic enantioselective synthesis of 19 new chiral alcohols with alkyl (C11-C19) and phenyl, substituted phenyl, heteroaromatic, and naphthyl groups 4a-4z with an (R)-configuration and high enan

Asymmetric synthesis of new chiral long chain alcohols

Yildiz, Tuelay,Yusufolu, Aye

experimental part, p. 2981 - 2987 (2011/03/20)

Sixteen new chiral alcohols with alkyl (C11-C19) and aryl, substituted aryl, hetero aryl and biaryl groups 2a-2t were synthesized by three different asymmetric reduction methods from their corresponding ketones 1a-1t. Chiral NaBHsub

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