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cis-3-phenyl-2-thiocarbamoyl-3,3a,4,5-tetrahydro-2H-benzindazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96814-47-0

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96814-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96814-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,1 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96814-47:
(7*9)+(6*6)+(5*8)+(4*1)+(3*4)+(2*4)+(1*7)=170
170 % 10 = 0
So 96814-47-0 is a valid CAS Registry Number.

96814-47-0Downstream Products

96814-47-0Relevant academic research and scientific papers

Synthesis, structure and antimicrobial evaluation of new 3,3a,4,5-tetrahydro-2H-benzo[g]indazol-2-yl-thiazol-4(5H)-ones

Gautam, Deepika,Chaudhary

, p. 219 - 226 (2015)

The reaction of semicarbazide or thiosemicarbazide with 2-arylidene-1-tetralones under alkaline condition affords 3,3a,4,5-tetrahydro- 2H-benzo[g]indazole-2-carbo(thio)amides as a mixture of cis and trans diastereoisomers of 3-H and 3a-H. The synthesis of

Isomerization of Substituted Tricyclic 4,5-Dihydropyrazoles

Lorand,Aradi,Szoelloesy,Toth,Konya

, p. 971 - 977 (2007/10/03)

The acid and base catalyzed isomerization of some tricyclic 2-pyrazolines with N-Carbamoyl-, N-thiocarbamoyl- and N-phenyl substituents was investigated. Starting from cis or trans 3-H, 3a-H diastereomers, equilibrium mixtures of cis and trans diastereomers were prepared which were separated and subsequently studied by 1H NMR and 13C NMR spectroscopy. A mechanism for the isomerization of the pyrazolines is suggested, supported by a deuterium exchange at C-3a.

Synthesis and Stereochemistry of Substituted Bi- and Tri-cyclic 4,5-Dihydropyrazoles

Lorand, Tamas,Szabo, Dezsoe,Foeldesi, Andras,Parkanyi, Laszlo,Kalman, Alajos,Neszmelyi, Andras

, p. 481 - 486 (2007/10/02)

A series of bi- and tricyclic 4,5-dihydropyrazoles have been studied by 1H n.m.r. and 13C n.m.r. spectroscopy and X-ray crystallography.They were synthesised by treating the corresponding mono- and dibenzylidenecycloalkanones and 2-benzylidene-3,4-dihydro

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