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86244-66-8

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86244-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86244-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,2,4 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86244-66:
(7*8)+(6*6)+(5*2)+(4*4)+(3*4)+(2*6)+(1*6)=148
148 % 10 = 8
So 86244-66-8 is a valid CAS Registry Number.

86244-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name tetraethyl octane-1,1,8,8-tetracarboxylate

1.2 Other means of identification

Product number -
Other names Octan-1,1,8,8-tetracarbonsaeure-tetraaethylester

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:86244-66-8 SDS

86244-66-8Relevant articles and documents

Process for the monoalkylation of C-H acid methylene groups

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Page/Page column 5 - 6, (2008/06/13)

The ratio of the alkali(ne earth) carbonate to the methylene group-containing substrate is above 0.6 : 1 in the monoalkylation of C-H acid methylene groups by reaction of the substrate in a polar aprotic solvent with a dihalogen compound having its halogens separated by a chain of at least3C and with reaction being in presence of the alkali(ne earth) carbonates and a phase transfer catalyst and being accompanied by continuous removal of the water formed. An Independent claim is also included for production of omega-haloalkyl-nitriles or -carboxylic acids by reacting a malonic acid diester or cyanoacetic ester with an alpha,omega-dihaloalkane as above and then saponifying and decarboxylating the product.

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