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144161-65-9

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144161-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144161-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,1,6 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144161-65:
(8*1)+(7*4)+(6*4)+(5*1)+(4*6)+(3*1)+(2*6)+(1*5)=109
109 % 10 = 9
So 144161-65-9 is a valid CAS Registry Number.

144161-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dichloropentan-2-yl phosphorodichloridate

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:144161-65-9 SDS

144161-65-9Upstream product

144161-65-9Downstream Products

144161-65-9Relevant articles and documents

SYNTHESIS OF 1,3-ALKADIENE-2-PHOSPHONATES

Gurevich, I. E.,Dogadina, A. V.,Sokolov, V. V.,Ionin, B. I.,Petrov, A. A.

, p. 47 - 55 (2007/10/02)

For the synthesis of 1,3-alkadiene-2-phosphonates, the oxidative chlorophosphorylation of allyl chlorides has been carried out, leading to the formation of 1,4-dichloroalkane-2-dichlorophosphonates.By the action of triethylamine on these compounds, one mole of HCl is eliminated from the 1-2 position.In order to obtain 1,3-diene systems, the 4-chloro-1-alkene-2-dichlorophosphonates that had been obtained in this manner were converted to the corresponding diethyl phosphonates, and a second mole of HCl was eliminated by the action of sodium tert-butylate.The structures of the intermediate and final products were established by means of 1H and 13C NMR spectroscopy. 1H-(31P) INDOR spectroscopy, and mass spectrometry.

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