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40438-23-1

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40438-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40438-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,3 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40438-23:
(7*4)+(6*0)+(5*4)+(4*3)+(3*8)+(2*2)+(1*3)=91
91 % 10 = 1
So 40438-23-1 is a valid CAS Registry Number.

40438-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-(triphenyl-λ<sup>5</sup>-phosphanylidene)carbamate

1.2 Other means of identification

Product number -
Other names (Triphenylphosphoranylidene)carbamic acid,methyl 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:40438-23-1 SDS

40438-23-1Relevant articles and documents

New Phosphonium Ylides by Functionalization of Triphenylphosphoranylideneacetamide

Wanner, Martin J.,Koomen, Gerrit-Jan

, p. 1513 - 1516 (2007/10/02)

Triphenylphosphoranylideneacetamide undergoes Michael reactions with several acceptors, giving rise, apart from the normal Michael adducts, to the formation of different products like glutarimide ylides and stabilized iminophosphoranes.Wittig reactions with these new ylides lead to a variety of α,β-unsaturated carbonyl compounds. Key Words: Stabilized phosphonium ylides, Wittig reaction, Michael reaction, Glutarimides.

Ester of (triarylphosphoranylidene)carbamic acid having diuretic and ability to lower plasma renin properties

-

, (2008/06/13)

Novel triarylphosphinimide derivatives having the formula STR1 wherein R1, R2 and R3 are each at the ortho or meta position, represent mono- or disubstituents and are selected from the group consisting of hydrogen, alkyl(C1 -C3), alkoxy(C1 -C3), trifluoromethyl and halogen; and R4 is selected from the group consisting of alkyl(C1 -C3), alkenyl(C2 -C3), alkynyl(C2 -C4), cycloalkyl(C3 -C5), cycloalkyl(C3 -C6)methyl, 4-oxopentyl, 3-tetrahydrofuranyl, 2,3-dihydro-1H-inden-1-yl, 1-alkyl(C1 -C3)cyclopentyl, trans-2-alkyl(C1 -C3)cyclopentyl, trans-2-alkoxy(C1 -C3)cyclopentyl, 1-cyclopropylethyl, 2-methylcyclopropylmethyl, dicyclopropylmethyl, 2-, 3- or 4-pyridinylmethyl, 2-cyclopenten-1-yl, tetrahydro-2H-pyran-4-yl and cis and trans-2-methoxycyclohexyl; with the proviso that when R4 is alkyl(C1 -C3), R1, R2 and R3 may not each be hydrogen STR2 wherein R1, R2 and R3 are each at the ortho or meta position and are selected from hydrogen and alkyl(C1 -C3), and X is an acid addition salt; processes for producing them, compositions containing them, and methods for using them in mammals to effect diuresis; to lower plasma renin levels and to increase cardiac contractility.

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