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42491-33-8

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42491-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42491-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,9 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42491-33:
(7*4)+(6*2)+(5*4)+(4*9)+(3*1)+(2*3)+(1*3)=108
108 % 10 = 8
So 42491-33-8 is a valid CAS Registry Number.

42491-33-8SDS

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 tert-butyl-bis(trimethylsilyl)phosphane

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:42491-33-8 SDS

42491-33-8Relevant articles and documents

Phosphacycloalkyldiones: synthesis and coordinative behaviour of 6- And 7-member cyclic diketophosphanyls

Pearce, Kyle G.,Simenok, Vladimir,Crossley, Ian R.

, p. 5482 - 5492 (2020/05/16)

Glutaryl and adipoyl chlorides undergo facile condensation with the bis(silyl)phosphanes RP(SiMe3)2(R = Me,nBu,tBu, Ph, Mes) to afford exclusively the phosphacycloalkyldiones (CH2)n(C)2PR (n= 3,4). Characterised spectroscopically and, for R = Ph, Mes (n= 3) crystallographically, the macrocycles are conformationally fluxional in solution and appreciably moisture sensitive. Though seemingly resistant to chemical oxidation at phosphorus, coordination is readily achieved, as illustrated by isolation oftrans-[Pt(PEt3){P(Ph)(CO)2(CH2)3}Cl2] and a series of tungsten pentacarbonyl complexes, which are characterised crystallographically and by infrared and NMR spectroscopy. Together, these data suggest the macrocycles to be relatively weak σ-donors with no appreciable π-acceptor character.

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