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3-(2-ETHYLPHENYL)CYCLOHEXANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898785-38-1

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898785-38-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898785-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,8 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 898785-38:
(8*8)+(7*9)+(6*8)+(5*7)+(4*8)+(3*5)+(2*3)+(1*8)=271
271 % 10 = 1
So 898785-38-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O/c1-2-11-6-3-4-9-14(11)12-7-5-8-13(15)10-12/h3-4,6,9,12H,2,5,7-8,10H2,1H3

898785-38-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-ethylphenyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 3-(2-ETHYLPHENYL)CYCLOHEXANONE

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:898785-38-1 SDS

898785-38-1Downstream Products

898785-38-1Relevant articles and documents

Sulfoxide-alkene hybrids: A new class of chiral ligands for the Hayashi-Miyaura reaction

Thaler, Tobias,Guo, Li-Na,Steib, Andreas K.,Raducan, Mihai,Karaghiosoff, Konstantin,Mayer, Peter,Knochel, Paul

supporting information; experimental part, p. 3182 - 3185 (2011/08/06)

Sulfoxide-alkene hybrids are introduced as a new class of chiral heterodentate ligands for the Hayashi-Miyaura reaction. The synthesis of these ligands was achieved without the use of protecting groups. A chiral resolution was performed via simple column-chromatographic separation of the diastereomeric ligands. Both diastereomers proved to be excellent ligands in Rh-catalyzed 1,4-addition reactions, furnishing chiral products with high enantioselectivities and, remarkably, opposite stereoconfigurations.

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