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88980-42-1

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88980-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88980-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,8 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88980-42:
(7*8)+(6*8)+(5*9)+(4*8)+(3*0)+(2*4)+(1*2)=191
191 % 10 = 1
So 88980-42-1 is a valid CAS Registry Number.

88980-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1'S)-1',2'-bis(methoxycarbonyl)ethyl 3-oxohexanoate

1.2 Other means of identification

Product number -
Other names (S)-2-(3-Oxo-hexanoyloxy)-succinic acid dimethyl ester

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:88980-42-1 SDS

88980-42-1Downstream Products

88980-42-1Relevant articles and documents

PREPARATION OF ACYLTETRONIC ACIDS USING t-BUTYL ACETOTHIOACETATE: TOTAL SYNTHESIS OF THE FUNGAL METABOLITES CAROLIC, CARLOSIC, AND CARLIC ACIDS

Booth, Paul M.,Fox, Christina, M. J.,Ley, Steve V.

, p. 121 - 130 (2007/10/02)

Dianions generated from S-t-butyl acetothioacetate ( 1 ) were alkylated with a variety of electrophiles at the γ-carbon centre.Treatment of the alkylated products with 2-hydroxy esters in the presence of silver(I) salts gave transesterified acetoacetate derivatives in good yields.These acetoacetates were cyclised efficiently to acyltetronic acid derivatives using tetrabutyl ammonium fluoride in THF solution at room temperature.By an appropriate choice of substituents the total synthesis of the fungal metabolite natural products carlosic, carolic, and carlic acids have been achieved.

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