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Benzenemethanol, α-1-hexenyl-α-methyl-, also known as 2-(1-hexenyl)-5-methylbenzenemethanol, is an organic compound with the molecular formula C14H24O. It is a derivative of benzyl alcohol, featuring a benzene ring with a methyl group at the α-position and a 1-hexenyl group attached to the same carbon. Benzenemethanol, a-1-hexenyl-a-methyl- is characterized by its unique structure, which combines the aromatic properties of the benzene ring with the aliphatic chain of the hexenyl group. It is used in the synthesis of various fragrances and pharmaceuticals due to its distinct scent and reactivity. The compound's properties, such as its boiling point, solubility, and stability, are influenced by the presence of the double bond in the hexenyl chain and the methyl group on the benzene ring, making it a versatile building block in organic chemistry.

821017-71-4

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821017-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 821017-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,1,0,1 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 821017-71:
(8*8)+(7*2)+(6*1)+(5*0)+(4*1)+(3*7)+(2*7)+(1*1)=124
124 % 10 = 4
So 821017-71-4 is a valid CAS Registry Number.

821017-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3-octene-2-ol

1.2 Other means of identification

Product number -
Other names 2-phenyloct-3-en-2-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:821017-71-4 SDS

821017-71-4Relevant academic research and scientific papers

Catalytic stereospecific allyl-allyl cross-coupling of internal allyl electrophiles with allylB(pin)

Le, Hai,Batten, Amanda,Morken, James P.

supporting information, p. 2096 - 2099 (2014/05/06)

Application of internal electrophiles in catalytic stereospecific allyl-allyl cross-coupling enable the rapid construction of multisubstituted 1,5-dienes, including those with all carbon quaternary centers. Compounds with minimal steric differentiation ca

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