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benzyl(methyl)diphenylphosphonium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63832-87-1

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63832-87-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63832-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 63832-87:
(7*6)+(6*3)+(5*8)+(4*3)+(3*2)+(2*8)+(1*7)=141
141 % 10 = 1
So 63832-87-1 is a valid CAS Registry Number.

63832-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl-methyl-diphenylphosphanium,iodide

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:63832-87-1 SDS

63832-87-1Relevant academic research and scientific papers

Titanium (IV) catalysis in the reduction of phosphine oxides

Coumbe, Tristan,Lawrence, Nicholas J.,Muhammad, Faiz

, p. 625 - 628 (2007/10/02)

Phosphine oxides can be reduced by triethoxysilane, or more conveniently polymethylhydrosiloxane, and catalytic titanium (IV) isopropoxide and provides a system for the efficient one-pot generation of phosphonium salts; the reduction occurs with retention of configuration at phosphorus.

Analytical Problems of the Reaction between Polymer Supported Phosphino Groups and Methyl Iodide

Paetzold, E.,Oehme, G.,Pracejus, H.

, p. 429 - 436 (2007/10/02)

A series of different crosslinked styrene-divinylbenzene-copolymers bearing diphenyl phosphinomethyl groups was reacted with methyl iodide in ethanol.The quaternization has been controlled by elementary analysis of P and I and by ir spectroscopy using a key band at 1123/cm.The spectroscopic method gave satisfactory results with sample amounts of 5 mg polymer in KBr discs.In resins containing up to 7 percent divinylbenzene the methylation was almost quantitative within 1 h refluxing.However, in highly crosslinked polymers (>10percent DVB) containing residues of free chloromethyl groups and intraresin quaternized phosphino groups we observed side reactions in boiling ethanol.These could be avoided by performing the methylation in toluene at room temperature.

Role of Through Space 2p-3d Overlap in the Alkylation of (ω-N,N-Dimethylaminoalkyl)diphenylphosphines and in the Alkaline Decomposition of Related Quaternary Phosphonium Salts

McEwen, William E.,Smith, Joanne H.,Woo, Edward J.

, p. 2746 - 2751 (2007/10/02)

A series of (ω-N.N-dimethylaminoalkyl)diphenylphosphines has been prepared and subjected to reaction with benzyl chloride in benzene-methanol (60:40 v/v) at 31.0 +/- 0.1 deg C.Each of quaternization reactions was found to follow the second-order rate law,

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