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61451-78-3

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61451-78-3 Usage

Chemical Properties

White to off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 61451-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,5 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61451-78:
(7*6)+(6*1)+(5*4)+(4*5)+(3*1)+(2*7)+(1*8)=113
113 % 10 = 3
So 61451-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H9O3P/c8-6-11(9,10)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,9,10)

61451-78-3SDS

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 hydroxymethoxy-oxo-phenylphosphanium

1.2 Other means of identification

Product number -
Other names hydroxymethoxy-oxo-phenylphosphonium

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:61451-78-3 SDS

61451-78-3Relevant articles and documents

Synthesis and structural characterization of a dimolybdenum complex bridged by the hydroxymethylphenylphosphinate ligand

Feng, Linsheng,Luck, Rudy L.

, p. 1317 - 1322 (2011)

Hydroxymethylphenylphosphinic acid, 1 was synthesized and structurally characterized by single crystal X-ray diffraction. Ligand 1 crystallized in the monoclinic P21 space group with two molecules comprising the unit cell and cell dimensions a

Synthesis of New Arylhydroxymethylphosphinic Acids and Derivatives

Cristau,Herve,Loiseau,Virieux

, p. 2216 - 2220 (2007/10/03)

The synthesis of a new series of arylhydroxymethylphosphinic acid derivatives is described. The protected compounds were prepared by a palladium(0) catalysed arylation of ethyl benzyloxymethylphosphinate with aryl halides. Subsequent hydrogenolysis of the

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