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54731-72-5

54731-72-5

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54731-72-5 Usage

Chemical Properties

Clear colorless to slightly yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 54731-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54731-72:
(7*5)+(6*4)+(5*7)+(4*3)+(3*1)+(2*7)+(1*2)=125
125 % 10 = 5
So 54731-72-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H11O4P/c1-7-9(6,8-2)4-3-5/h5H,3-4H2,1-2H3

54731-72-5 Well-known Company Product Price

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  • TCI America

  • (H0779)  Dimethyl (2-Hydroxyethyl)phosphonate  >92.0%(GC)

  • 54731-72-5

  • 5g

  • 745.00CNY

  • Detail

  • TCI America

  • (H0779)  Dimethyl (2-Hydroxyethyl)phosphonate  >92.0%(GC)

  • 54731-72-5

  • 25g

  • 2,550.00CNY

  • Detail

54731-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Dimethyl 2-hydroxyethylphosphonate

1.2 Other means of identification

Product number -
Other names 2-dimethoxyphosphorylethanol

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:54731-72-5 SDS

54731-72-5Relevant articles and documents

SYNTHESIS AND PHARMACOLOGICAL ACTIVITY OF ALKYLPHOSPHONIC AND OXY DERIVATIVES

Tyurenkov, I. N.,Brel', A. K.,Strel'tsova, G. V.,Skladonovskaya, N. N.,Nazarenko, V. N.

, p. 120 - 123 (1988)

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Boutevin,Hervaud,Jeanmaire,Boulahna,Elasri

, p. 1 - 14 (2007/10/03)

This paper describes the synthesis and the characterization by 1H and 31P NMR of several monosalts and monoacids issued from phosphonates bearing alkyl groups (C1 to C18) or alkylene groups (allyl or vinyl). Functional compounds (alcohol or acetate) were also used and the results demonstrate the reaction selectivity. The method involves sodium iodide in ketones (acetone or 2-butanone) under reflux. It is very selective for monosalts, but only methyl phosphonates are very reactive. The corresponding acids were then obtained in quantitative yields with a cation exchange resin (sulfate acid).

Note on the Synthesis of β-Hydroxyethanephosphonic Acid

Gloede, J.,Weigt, E.,Gross, H.

, p. 327 - 328 (2007/10/02)

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