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20394-86-9

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20394-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20394-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,9 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20394-86:
(7*2)+(6*0)+(5*3)+(4*9)+(3*4)+(2*8)+(1*6)=99
99 % 10 = 9
So 20394-86-9 is a valid CAS Registry Number.

20394-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-methyl-phosphinic acid

1.2 Other means of identification

Product number -
Other names benzylphosphinic acid

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:20394-86-9 SDS

20394-86-9Relevant articles and documents

Synthesis of alkyl phosphinic acids from silyl phosphonites and alkyl halides

Boyd, E. Andrew,Regan, Andrew C.,James, Keith

, p. 4223 - 4226 (1994)

Mono- and di-substituted phosphinic acids have been synthesised in a one-pot reaction, by the addition of alkyl halides to silyl phosphonites, under mild and flexible conditions.

Rapid and efficient synthesis of unsymmetrical phosphinic acids r′t(o)ohr″

Fougere, Cecile,Guenin, Erwann,Hardouin, Julie,Lecouvey, Marc

experimental part, p. 6048 - 6054 (2010/03/02)

A new synthesis of unsymmetrical phosphinic acids R′P(O)OHR″ has been evaluated, The first P-C bond was formed by base-promoted H-phosphinate alkylation of a protected H-phosphinate, which is easier and safer to handle, A onepot methodology was developed for the second P-C bond formation reaction that: involves the sila-Arbuzov reaction. This methodology was then extended to the synthesis of a dialkylphosphinic acid with an amino functionality.

Efficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinate

Kalek, Marcin,Stawinski, Jacek

experimental part, p. 10406 - 10412 (2010/02/27)

A general, efficient method for the microwave-assisted synthesis of mono- and diarylphosphinic acids from anilinium phosphinate and aryl halides, using Pd(0) and Xantphos as a supporting ligand, was developed.

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