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dibutyl phosphonite is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30653-71-5

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30653-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30653-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30653-71:
(7*3)+(6*0)+(5*6)+(4*5)+(3*3)+(2*7)+(1*1)=95
95 % 10 = 5
So 30653-71-5 is a valid CAS Registry Number.

30653-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutoxyphosphane

1.2 Other means of identification

Product number -
Other names dibutoxyphosphonite

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:30653-71-5 SDS

30653-71-5Relevant academic research and scientific papers

Synthesis and reactivity of substituted α-carbonylphosphonites and their derivatives

Prishchenko, Andrey A.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Petrosyan, Valery S.

experimental part, p. 352 - 372 (2012/08/28)

Convenient methods for the synthesis of functionalized organophosphorus compounds containing carbonyl groups as well as di- or trialkoxymethyl fragments attached to phosphorus, and their derivatives, starting from the available derivatives of trivalent phosphorus acids, are proposed, and some properties of the new functionalized organophosphorus compounds are presented. So, the alkylation and acylation reaction of (dialkoxymethyl) phosphonites and their analogs have been studied. It is found that the Arbuzov rearrangement of these compounds was accompanied by the phosphorus-carbon bond cleavage with unique retention of the three-coordinate phosphorus.

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