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90601-12-0

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90601-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90601-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90601-12:
(7*9)+(6*0)+(5*6)+(4*0)+(3*1)+(2*1)+(1*2)=100
100 % 10 = 0
So 90601-12-0 is a valid CAS Registry Number.

90601-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Phosphonium, [2-(dimethylamino)-1-methylethenyl]triphenyl-, chloride (1:1)

1.2 Other means of identification

Product number -
Other names Phosphonium, [2-(dimethylamino)-1-methylethenyl]triphenyl-, chloride

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:90601-12-0 SDS

90601-12-0Relevant articles and documents

Reactions with Phosphine Alkylenes, XLV. Reactions of Alkylidenetriphenylphosphoranes with Tetramethylformamidinium Chloride. Synthesis of triphenylphosphonium Chloride and (Formylalkylidene)triphenylphosphoranes

Bestmann, Hans Juergen,Schmid, Guenter,Oechsner, Helmut,Ermann, Peter

, p. 1561 - 1571 (2007/10/02)

Phosphonium ylides 1 react with tetramethylformamidinium chloride (2) to form enamine phosphonium chlorides 8 and the formic orthoamide 7.The salts 8 show temperature depending 1H NMR spectra with respect to the protons of the dimethylamino group (hindered rotation around the C - N(CH3)2 bond).Treatment of 8 with acids and subsequently with bases gives rise to the formation of the formyl ylides 19. 8a is deprotonated with sodium amide to give the phosphaallene ylide 20, which reacts with water to yield the phosphane oxide 21, and with methyl iodide stereospecifically to form 8b.

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