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decyl diphenyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14167-87-4

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14167-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14167-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14167-87:
(7*1)+(6*4)+(5*1)+(4*6)+(3*7)+(2*8)+(1*7)=104
104 % 10 = 4
So 14167-87-4 is a valid CAS Registry Number.

14167-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name decyl diphenyl phosphate

1.2 Other means of identification

Product number -
Other names Phosphorsaeure-decylester-diphenylester

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:14167-87-4 SDS

14167-87-4Downstream Products

14167-87-4Relevant academic research and scientific papers

A simple, general and improved procedure for phosphorylation of alcohols catalyzed by indium(III) chloride

Ranu, Brindaban C.,Das, Arijit

, p. 1063 - 1064 (2007/10/03)

A general and efficient procedure has been developed for the preparation of dialkyl phosphate esters by indium(III) chloride catalyzed phosphoryl transfer from diethyl and diphenyl chlorophosphate to a variety of alcohols and phenols in THF in presence of triethylamine.

TRANSITION METHAL-CATALYZED SUBSTITUTION REACTION OF ALLYLIC PHOSPHATES WITH GRIGNARD REAGENTS

Yanagisawa, Akira,Nomura, Nobuyoshi,Yamamoto, Hisashi

, p. 6017 - 6028 (2007/10/02)

SN2-selective Grignard coupling with primary allylic diphenylphosphates was successfully achieved using Ni or Fe catalyst.In sharp contrast, a catalytic amount of CuCN*2LiCl promoted a SN2'-selective coupling reaction.In the presence of the copper catalyst, stereochemically homogeneous γ-disubstituted allyl Grignard reagents reacted at the less substituted allylic terminus (α-position) with an allylic diphenylphosphate selectively without losing the double bond geometry.

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