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Phosphonic acid, (1-hydroxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20188-02-7

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20188-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20188-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,8 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20188-02:
(7*2)+(6*0)+(5*1)+(4*8)+(3*8)+(2*0)+(1*2)=77
77 % 10 = 7
So 20188-02-7 is a valid CAS Registry Number.

20188-02-7SDS

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-hydroxyethylphosphonic acid

1.2 Other means of identification

Product number -
Other names Oxyaethyl-phosphinsaeure

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:20188-02-7 SDS

20188-02-7Upstream product

20188-02-7Relevant academic research and scientific papers

The formation of α-amino- and α-hydroxy-alkanephosphonic acids in the reactions of phosphite esters with aldehydes and alkyl carbamates

Hudson, Harry R.,Ismail, Fatima,Pianka, Max,Wan, Chi-Wai

, p. 245 - 257 (2007/10/03)

The preparation of α-aminoalkanephosphonic acids from triphenyl phosphite, an aldehyde, and ethyl or benzyl carbamate in glacial acetic acid, followed by hydrolysis, is accompanied by the formation of the corresponding α-hydroxyphosphonic acid. Reaction in toluene, using boron trifluoride-etherate as catalyst, affords an alternative preparative procedure but does not prevent the formation of α-hydroxyphosphonic acid. 31P nmr reveals the presence of numerous intermediates. The reactions are discussed.

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