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(Z)-2-Benzyliden-4,5,6,7-tetrahydro-1-methylindolin-3-on is a complex organic compound with the molecular formula C16H17NO. It is a derivative of indolin-3-on, featuring a benzylidene group at the 2-position and a methyl group at the 1-position. (Z)-2-Benzyliden-4,5,6,7-tetrahydro-1-methylindolin-3-on is characterized by its unique structure, which includes a tetrahydroindoline core with a double bond between the 2nd and 3rd carbon atoms, giving it the (Z)-configuration. It is synthesized through various chemical reactions and is used in the pharmaceutical and chemical industries for the development of potential drug candidates and other organic compounds. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest for researchers in organic chemistry.

74477-69-3

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74477-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74477-69-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,7 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74477-69:
(7*7)+(6*4)+(5*4)+(4*7)+(3*7)+(2*6)+(1*9)=163
163 % 10 = 3
So 74477-69-3 is a valid CAS Registry Number.

74477-69-3Downstream Products

74477-69-3Relevant academic research and scientific papers

Syntheses and Properties of Pyrrolindigo Compounds

Pfeiffer, Georg,Bauer, Helmut

, p. 564 - 589 (2007/10/02)

4,4',5,5',6,6',7,7'-Octahydroindigo (9c), 4,4'-dibutyl-5,5'-dimethylpyrrolindigo (9a) and di(cyclopenta)pyrrolindigo (9d) as well as the condensation products from 2-pyrrolin-4-ones with benzaldehyde, isatin, glyoxale, and 2-methoxy-3-indolone, plus N-methyl- and N,N'-dimethylderivatives of 9c and tetrahydroindigo 31 were all synthesized and compared with other indigoids especially the corresponding benzoannelated compounds.The unusul behavior of N-methylindigoids is discussed.In the boron chelate 39 of 1-methyl-4,5,6,7-tetrahydroindigo the structure of a fixed tautomeric indigo is approached.

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