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142397-12-4

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142397-12-4 Usage

Chemical structure

The compound has a complex structure with a triazolopyridine ring fused with a carbonitrile group and a dihydrophenylnitrophenyl group.

Potential applications

It may have potential pharmaceutical applications due to its unique structure and properties.

Areas of interest

Its synthesis and potential biological activities are areas of interest for further research.

Molecular weight

The molecular weight of this compound is approximately 348.32 g/mol.

Appearance

The appearance of this compound is not specified in the material provided.

Solubility

The solubility of this compound is not specified in the material provided.

Stability

The stability of this compound is not specified in the material provided.

Reactivity

The reactivity of this compound is not specified in the material provided.

Hazards

The hazards associated with this compound are not specified in the material provided.

Storage

The storage requirements for this compound are not specified in the material provided.

Handling

The handling precautions for this compound are not specified in the material provided.

Check Digit Verification of cas no

The CAS Registry Mumber 142397-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,3,9 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 142397-12:
(8*1)+(7*4)+(6*2)+(5*3)+(4*9)+(3*7)+(2*1)+(1*2)=124
124 % 10 = 4
So 142397-12-4 is a valid CAS Registry Number.

142397-12-4Downstream Products

142397-12-4Relevant articles and documents

Reactions of 1,3-Dipoles with Heterocycles, 8. - Synthesis of 1,8a-Dihydrotriazolopyridines and Benzologues

Grubert, Lutz,Jugelt, Werner,Bress, Hans Joachim,Koeppel, Hubert,Strietzel, Ute,Dombrowski, Anke

, p. 885 - 894 (2007/10/02)

The C,N double bond of pyridine, quinoline and isoquinoline as heterodipolarophile react with diarylnitrilimines 2, generated in situ by dehydrohalogenation of N-phenylbenzhydrazonoyl chlorides 1, in a cycloaddition with complete regioselectivity.A facile

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