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Benzenemethanol, 2-(2E)-2-butenyl- (9CI), also known as 2-(2E)-2-butenylbenzenemethanol or 2-allylphenylmethanol, is an organic compound with the chemical formula C11H14O. It is a colorless to pale yellow liquid with a strong, sweet, floral odor. Benzenemethanol, 2-(2E)-2-butenyl- (9CI) is characterized by the presence of a benzene ring with a hydroxyl group (-OH) attached to the carbon atom at position 2, and a 2-butenyl (allyl) group attached to the same carbon atom. The 2-butenyl group is in the E configuration, indicating that the double bond is in the trans position. This chemical is used in the synthesis of various pharmaceuticals, agrochemicals, and fragrances due to its unique chemical structure and properties.

82316-08-3

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82316-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82316-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,1 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82316-08:
(7*8)+(6*2)+(5*3)+(4*1)+(3*6)+(2*0)+(1*8)=113
113 % 10 = 3
So 82316-08-3 is a valid CAS Registry Number.

82316-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((E)-but-2-en-1-yl)benzyl alcohol

1.2 Other means of identification

Product number -
Other names [((E)-2-But-2-enyl)-phenyl]-methanol

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:82316-08-3 SDS

82316-08-3Relevant academic research and scientific papers

Cyclization of aryl acyl radicals generated from S-(4-cyano)phenyl thiolesters by a nickel complex catalyzed electroreduction

Ozaki, Shigeko,Adachi, Masashi,Sekiya, Sayaka,Kamikawa, Rie

, p. 4586 - 4589 (2007/10/03)

Aromatic acyl radicals generated from S-(4-cyano)phenyl 2-alkenylthiobenzoate by a nickel complex catalyzed electroreduction undergo 5- and 6-exo cyclization to give 1-indanone and dihydro-1-naphthalenone derivatives, respectively.

Intramolecular addition reactions of functionalized arylcarbenes to double bonds

Kirmse, Wolfgang,H?mberger, Günter

, p. 3925 - 3934 (2007/10/02)

Arylcarbenes with unsaturated ortho substituents (vinyloxy, 1-propenyloxy, allyl, 2-butenyl, 2,4-pentadienyl) were generated in methanol by photolysis of diazo precursors. Intermolecular OH insertion was found to compete with intramolecular addition to th

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