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1-Cyclohexen-1-ol, 2-(phenylmethyl)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81418-18-0

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81418-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81418-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81418-18:
(7*8)+(6*1)+(5*4)+(4*1)+(3*8)+(2*1)+(1*8)=120
120 % 10 = 0
So 81418-18-0 is a valid CAS Registry Number.

81418-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,2-benzylcyclohexen-1-ol

1.2 Other means of identification

Product number -
Other names 1-acetoxy-2-benzylcyclohexene

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:81418-18-0 SDS

81418-18-0Relevant academic research and scientific papers

Enol Acetates: Versatile Substrates for the Enantioselective Intermolecular Tsuji Allylation

Liu, Ji,Mishra, Sourabh,Aponick, Aaron

supporting information, p. 16152 - 16158 (2018/12/13)

A highly versatile enantioselective intermolecular Tsuji allylation that generates alpha-quaternary stereocenters is reported. The methodology utilizes a prochiral enol acetate as a substrate, which is the last class of the original Tsuji substrates to be

Enantioface-differentiating protonation with chiral γ-hydroxyselenoxides

Takahashi, Tamiko,Nakao, Naoki,Koizumi, Toru

, p. 3293 - 3308 (2007/10/03)

Enantioface-differentiating protonation of a chiral metal enolates of α-alkylcarbonyl compounds 7 has been developed using chiral γ-hydroxyselenoxides 1 as a proton source. Reaction of zinc bromide enolates of 2-benzyl- and 2-n-propylcyclohexanones with (S(Se))-1e gave (S)-2-benzylcyclohexanone 7a and (R)-2-n-propylcyclohexanone 7c in high enantiomeric excess, respectively. Intramolecular hydrogen bonding of the selenoxide 1, chelation effects between 1 and metal enolate, and 2-exo-hydroxy-10-bornyl-framework could contribute to this asymmetric induction.

Enzyme-mediated enantioface-differentiating hydrolysis of α-substituted cycloalkanone enol esters

Matsumoto, Kazutsugu,Tsutsumi, Seiji,Ihori, Tamiko,Ohta, Hiromichi

, p. 9614 - 9619 (2007/10/02)

A new type of enzymatic hydrolysis, enantioface-differentiating hydrolysis of enol esters, is disclosed. As a result of screening, Pichia miso IAM 4682, a type of yeast, was selected as the best strain to perform the enantioselective hydrolysis of enol esters to give α-chiral ketones. For example, incubation of 1-acetoxy-2-methylcyclohexene (4a) with P. miso afforded (S)-2-methylcyclohexanone (5) in high optical yield. This enzymatic hydrolysis is applicable to various α-substituted cycloalkanone enol esters, and thereby chiral six-, eight-, ten-, and twelve-membered-ring ketones of 70-96% enantiomeric excess (ee) are easily prepared.

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