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1116086-46-4

1116086-46-4

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1116086-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1116086-46-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,6,0,8 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1116086-46:
(9*1)+(8*1)+(7*1)+(6*6)+(5*0)+(4*8)+(3*6)+(2*4)+(1*6)=124
124 % 10 = 4
So 1116086-46-4 is a valid CAS Registry Number.

1116086-46-4SDS

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 (R)-ibuprofen di(1-naphthyl)methyl ester

1.2 Other means of identification

Product number -
Other names -

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:1116086-46-4 SDS

1116086-46-4Downstream Products

1116086-46-4Relevant articles and documents

Method for manufacturing optically active carboxylic acid ester

-

Page/Page column 10; 11; 12; 13; 14, (2016/05/11)

A method that manufacturers an optically active carboxylic acid ester at high yield and high enantioselectivity is provided. An optically active carboxylic acid ester is manufactured at high yield and high enantioselectivity by reacting a racemic carboxyl

Homobenzotetramisole-catalyzed kinetic resolution of α-Aryl-, α-Aryloxy-, and α-Arylthioalkanoic acids

Yang, Xing,Birman, Vladimir B.

supporting information; experimental part, p. 2301 - 2304 (2010/01/19)

Effective kinetic resolutions of α-aryl-, αaryloxy-, and α-arylthioalkanoic acids have been achieved via in situ generation of their symmetrical anhydrides and enantioselective alcoholysis in the presence of homobenzotetramisole (HBTM) 3.

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