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75238-99-2

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75238-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75238-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75238-99:
(7*7)+(6*5)+(5*2)+(4*3)+(3*8)+(2*9)+(1*9)=152
152 % 10 = 2
So 75238-99-2 is a valid CAS Registry Number.

75238-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-4,6-diphenyl-1H-pyridine-3,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 1,2-dihydro-2-oxo-4,6-diphenyl-3,5-pyridinedicarbonitrile

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:75238-99-2 SDS

75238-99-2Relevant articles and documents

Reactivity of Heterocyclic Compounds. VI. 2,6-Diaminopyrimidine-5-carbonitriles and 3,5-Dicyanopyridones from 2-Amino-4H-pyran-3,5-dicarbonitriles

Seoane, C.,Soto, J. L.,Quinteiro, M.

, p. 35 - 41 (2007/10/02)

The reaction of different 2-amino-4H-pyrans (1, 10) with guanidine affords 2,6-diaminopyrimidine derivatives (3).Treatment of the pyrans mentioned or their acetylated derivatives with trityl tetrafluoroborate does not yield pyrylium salts, and pyrid-2-one

Synthesis of Heterocyclic Compounds, XXXVII Preparation of 4,6-Diaryl-1,2-dihydro-2-thioxo-3,5-pyridinedicarbonitriles and Related Compounds

Encinas, Maria Jesus Rubio,Seoane, Carlos,Soto, Jose L.

, p. 213 - 222 (2007/10/02)

The reaction of cyanothioacetamide (1) with α-benzoylcinnamonitriles 2 in basic ethanolic solution leads to 4,6-diaryl-1,2-dihydro-2-thioxo-3,5-pyridinedicarbonitriles 3 together with the disulfides 4.Treatment of 4 with 2-mercaptoethanol causes transformation into 3 which can lead to 4 upon reaction with either iodine-potassium iodide or dimethyl sulfoxide-trifluoroacetic acid.Methylation of 3 or 4 yields the expected methylthiopyridines 5.On the other hand, reaction of 3 with methyl chloroacetate allows the preparation of thienopyridines 8.

Ring Transformations of 4H-Pyrans. Pyridines from 2-Amino-4H-Pyrans

Seoane, Carlos,Soto, Jose L.,Zamorano, Pilar,Quinteiro, Margarita

, p. 309 - 314 (2007/10/02)

Ring transformations of 4H-pyrans into pyridines are reported.Treatment of 2-amino-4,6-diaryl-3,5-dicyano-4H-pyrans (I) with nitrosylsulfuric acid brings about their transformation into 3,5-dicyano-4,6-diaryl-2-pyridones (VI) which can also be obtained fr

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