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Benzoesaeure-ethylester-<4-nitro-phenylhydrazid>, also known as ethyl 4-nitrophenylhydrazinecarboxylate, is a chemical compound with the molecular formula C9H10N2O4. It is a derivative of benzoic acid, where the carboxyl group is esterified with ethanol, and the phenyl ring is substituted with a 4-nitro group and a hydrazine group. Benzoesaeure-ethylester-<4-nitro-phenylhydrazid> is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and other chemicals. It is important to handle Benzoesaeure-ethylester-<4-nitro-phenylhydrazid> with care due to its potential reactivity and the presence of a nitro group, which can be associated with explosive properties under certain conditions.

967-73-7

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967-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 967-73-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 967-73:
(5*9)+(4*6)+(3*7)+(2*7)+(1*3)=107
107 % 10 = 7
So 967-73-7 is a valid CAS Registry Number.

967-73-7Downstream Products

967-73-7Relevant articles and documents

REACTION OF BENZONITRILE N-(p-NITROPHENYL)IMIDE WITH 5-SUBSTITUTED TETRAZOLES: A NEW ROUTE TO SUBSTITUTED 1,2,4-TRIAZOLES VIA N-HYDRAZONOYLTETRAZOLES

Butler, Richard N.,Fitzgerald, Kevin J.

, p. 1587 - 1592 (2007/10/02)

A wide range of phenyl 5-R-substituted (R = aryl, alkyl, amino, halo, H) 1- and 2-hydrazonoyltetrazoles has been synthesized.Substituent effects on the orientation of nitrile imide attack on 5-aryltetrazoles are reported.Thermolysis and fragmentation of t

1-Hydrazonyltetrazoles: Fragmentative Cyclisation - A New Route to Substituted 1,2,4-Triazoles.

Butler, Richard N.,Fitzgerald, Kevin J.,Fleming, Mary T.

, p. 4921 - 4922 (2007/10/02)

The reaction of tetrazole and some 5-aminotetrazoles with C-phenyl-N-4-nitrophenyl-nitrileimine gave 1-hydrazonyltetrazoles which fragmented and cyclised to 1,2,4-triazoles with overall loss of HN3.

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