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Phosphine, (2-methyl-1-propenyl)diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34193-25-4

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34193-25-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34193-25-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,9 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34193-25:
(7*3)+(6*4)+(5*1)+(4*9)+(3*3)+(2*2)+(1*5)=104
104 % 10 = 4
So 34193-25-4 is a valid CAS Registry Number.

34193-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Diphenyl(2-methyl-1-propenyl)phosphine

1.2 Other means of identification

Product number -
Other names (2-methyl-1-propenyl)-diphenyl-phosphine

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:34193-25-4 SDS

34193-25-4Downstream Products

34193-25-4Relevant academic research and scientific papers

The reaction of 1-chloro-2-methyl-2-propenyllithium with a selection of organolithiums. The development and synthetic utility of novel base/nucleophile combinations

Nelson, Donna J.,Nagarajan, Ananthanarayanan

, p. 1 - 6 (1993)

The title compound was generated by and reacted with (1) a series of reagents which have basic as well as nucleophilic properties and (2) a series of base/nucleophile combinations.Product yields of the isobutenyl derivative were generally low to very good, and the best results (89percent) were obtained by using a 1:2 ratio (3 equiv total) of nBuLi:LiPPh2.Synthetic utility of the reaction is optimized as it approaches a situation in which the base/nucleophile combination is composed of one compound which is both a strong base and a poor nucleophile and another compound which is both a weak base and a good nucleophile.

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