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23731-39-7

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23731-39-7 Usage

Uses

Methyl-d3 Formate (CAS# 23731-39-7) is a useful isotopically labeled research compound.

Check Digit Verification of cas no

The CAS Registry Mumber 23731-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,3 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 23731-39:
(7*2)+(6*3)+(5*7)+(4*3)+(3*1)+(2*3)+(1*9)=97
97 % 10 = 7
So 23731-39-7 is a valid CAS Registry Number.

23731-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL-D3 FORMATE

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:23731-39-7 SDS

23731-39-7Relevant articles and documents

Cascade catalysis for the homogeneous hydrogenation of CO2 to methanol

Huff, Chelsea A.,Sanford, Melanie S.

supporting information; experimental part, p. 18122 - 18125 (2012/01/04)

This communication demonstrates the homogeneous hydrogenation of CO 2 to CH3OH via cascade catalysis. Three different homogeneous catalysts, (PMe3)4Ru(Cl)(OAc), Sc(OTf) 3, and (PNN)Ru(CO)(H), operate in sequence to promote this transformation.

Bis(dimethoxymethyl) peroxide and bis(1,1-dimethoxyethyl) peroxide

Kopeczky, Karl R.,Molina, Jose

, p. 2350 - 2355 (2007/10/02)

The title compounds 1 and 2, the first examples of peroxides polysubstituted at the α and α' positions by alkoxy groups, are formed by benzophenone sensitized photooxygenation of trimethoxymethane and 1,1,1-trimethoxyethane, respectively.No peroxide was formed from tetramethoxymethane.Allowing 98percent hydrogen peroxide and trimethylmethane to stand results in an 80percent yield of 1, so that 1 and 2 are probably formed by such a disproportionation reaction during photooxygenation.Compound 1 is converted quantitatively to methanol, methyl formate, and dimethyl carbonate in pyridine solution at 60 deg C.In acidic methanol both 1 and 2 undergo solvolysis rapidly with exclusive cleavage of the carbon - peroxy oxygen bond.Signals for the ether and peroxy oxygens of 1 appear at 34 and 263 ppm and those of 2 appear at 40 and 264 ppm in the 17O nuclear magnetic resonance spectrum.Luminescence results when 1 and 2 are heated to 150 deg C.

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