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Imidodicarbonicdiamide, 2-methyl-N,N'-diphenyl-, also known as 2-methyl-N,N'-diphenyl-imidodicarbonicdiamide or MDIP, is an organic compound with the chemical formula C15H14N4O2. It is a white crystalline solid that is soluble in organic solvents such as ethanol, acetone, and dimethyl sulfoxide. MDIP is a derivative of imidodicarbonic diamide, which is a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is characterized by its 2-methyl group and diphenyl substituents on the imidodicarbonic diamide backbone, which contribute to its unique chemical properties and potential applications in the development of new drugs and pesticides.

1034-09-9

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1034-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034-09-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1034-09:
(6*1)+(5*0)+(4*3)+(3*4)+(2*0)+(1*9)=39
39 % 10 = 9
So 1034-09-9 is a valid CAS Registry Number.

1034-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methyl-N-phenylcarbamoyl-N'-phenyl-harnstoff

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1034-09-9 SDS

1034-09-9Downstream Products

1034-09-9Relevant academic research and scientific papers

ZUR FRAGE DER EXISTENZ VON ACYL-SELENOCYANATEN SYNTHESE UND REAKTIONEN VON 2-ALKYL-4-ARYL-ALLOPHANOYL-SELENOCYANATEN /1,2/

Werchan, Hans Georg,Dittrich, Guenter

, p. 2833 - 2834 (2007/10/02)

2-Alkyl-4-aryl-allophanoyl selenocyanates were synthesized by interaction of correspondingly substituted allophanoyl chlorides with alkali selenocyanates forming stable representatives of the yet nearly unknown class of acyl selenocyanates.

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