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88682-34-2

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88682-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88682-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,8 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88682-34:
(7*8)+(6*8)+(5*6)+(4*8)+(3*2)+(2*3)+(1*4)=182
182 % 10 = 2
So 88682-34-2 is a valid CAS Registry Number.

88682-34-2SDS

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 2,3-dihydro-1,1,3,3-tetraphenyl-1,3-diphosphoniaindene dibromide

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:88682-34-2 SDS

88682-34-2Relevant articles and documents

Carbodiphosphorane Isomers Based on a 1,3-Diphosphaindane Skeleton, and Their Precursors

Bowmaker, Graham A.,Herr, Rudolf,Schmidbaur, Hubert

, p. 3567 - 3579 (2007/10/02)

In a search for ring-strained carbodiphosphoranes , the diastereomeric bis-phosphanes 1a(RR, SS, RS) and the symmetrical analogue 1c have been converted into the corresponding cyclic methylene-bridged bis-phosphonium bromides 2a,c and hexafluorophosphates 2b. 2a(RR;SS) and 2a(RS) were separated by fractional crystallization.Treatment of 2a-c with base (NH3 or n-BuLi) yields, in a first step, the semi-ylide salts 3a-c which, unexpectedly, undergo hydrolytic or ammonolytic cleavage at the ylidic PCHP bridge resulting in formation of the phosphane oxide or phosphane imine salts 5a, c and 6a, respectively.The second deprotonation step, using (C2H5)3P=CHCH3 as a transylidating agent, affords the conjugated bis-ylide 7a in the case of 2a, 3a(RS), but gives the carbodiphosphorane 4c in the case of the methyl-free 2c, 3c.With n-BuLi, 2a(RS) also yields the analogous species 4a(RS), probably as an Li(+) adduct, as proven by its conversion into the symmetrical methylated product 8a(RS).- 1c is methylated with CH3I at one P centre only.The resulting phosphonium salt 10 gives the mono-ylide 11 on treatment with NaNH2.

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