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Phosphonic acid, [1-methyl-1-[[(phenylamino)carbonyl]amino]ethyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100967-69-9

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100967-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100967-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,9,6 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100967-69:
(8*1)+(7*0)+(6*0)+(5*9)+(4*6)+(3*7)+(2*6)+(1*9)=119
119 % 10 = 9
So 100967-69-9 is a valid CAS Registry Number.

100967-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [α-(N'-phenyl-ureido)-isopropyl]-phosphonic acid diethyl ester

1.2 Other means of identification

Product number -
Other names [α-(N'-Phenyl-ureido)-isopropyl]-phosphonsaeure-diaethylester

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:100967-69-9 SDS

100967-69-9Downstream Products

100967-69-9Relevant academic research and scientific papers

Study on the kinetics of the reaction between diethyl ester of 1-amino-methyl-ethanephosphonic acid and phenyl isocyanate

Alexiev, Alexi,Lachkova, Victoria,Petrov, Galin

, p. 191 - 199 (1997)

The kinetics of the reaction between O,O-diethyl ester of 1-amino-1-methyl-ethane phosphonic acid and phenylisocyanate, producing diethyl ester of 1-methyl-1-(N-phenylcarbamoyl-amino)ethane phosphonic acid is studied by IR spectroscopy. It is established that the reaction is of second order. The probable scheme of the reaction mechanism is suggested. The rate constant k of the initial stage of the reaction is determined. It is established that the rate constant is increased at the advanced stage of the process. The observed enhancement is ascribed to the autocalalytic effect of the reaction product.

SYNTHESIS OF 1-METHYL-1-(N-SUBSTITUTED CARBAMOYL- AND THIOCARBAMOYL-AMINO) ALKANEPHOSPHONIC ACIDS-DIETHYL ESTERS

Lachkova, Victoria I.,Petrov, Galin,Hussein, Ali H.

, p. 161 - 168 (2007/10/02)

Diethylesters of 1-methyl-1-(N-substituted carbamoyl- or thiocarbamoyl-amino)-alkane-phosphonic acids are obtained by interaction of O,O-diethyl esters of 1-amino-1-methyl-alkanephosphonic acids and different isocyanates or isothiocyanates at room tempera

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