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methyl 2,2,3,3-tetramethoxypropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92095-79-9

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92095-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92095-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,9 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92095-79:
(7*9)+(6*2)+(5*0)+(4*9)+(3*5)+(2*7)+(1*9)=149
149 % 10 = 9
So 92095-79-9 is a valid CAS Registry Number.

92095-79-9SDS

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 methyl 2,2,3,3-tetramethoxypropanoate

1.2 Other means of identification

Product number -
Other names 2,2,3,3-Tetramethoxy-propionsaeuremethylester

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:92095-79-9 SDS

92095-79-9Downstream Products

92095-79-9Relevant academic research and scientific papers

SYNTHESIS OF PROTECTED α-KETOESTER DERIVATIVES USING SILYL KETENE ACETALS OF ALKYL DIALKOXYACETATES

Malhiac, Catherine,Tekin, Jacques,Ramiandrasoa, Guy,Leveque, Hubert,Combret, Jean-Claude

, p. 127 - 132 (2007/10/02)

Two readily accessible (RO)2, C=C(OSiMe3)(OR) react smoothly with oxygenated electrophiles (aldehydes, ketals, orthoesters) leading,, with good yields, to the corresponding β-functionalized α,α dialkoxyesters. Key words: 1,2,2 trialkoxy-1-trimethylsilylox

LITHIOPENTAMETHOXYCYCLOPROPANE: PRECURSOR FOR THE SYNTHESIS OF HIGHLY OXYGENATED CYCLOPROPANES

Moss, Robert A.,Hui, Henry K.

, p. 305 - 312 (2007/10/02)

Pentamethoxychlorocyclopropane (1) affords the corresponding lithiocyclopropane (2) upon treatment with t-butyllithium.Reagent 2 can be quenched with H2O, MeI, Me3SiCl, or MeSSMe to give excellent yields of highly oxygenated cyclopropanes 3-6.

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