Cas 478031-79-7,1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE

478031-79-7

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Basic information

Product Name: 1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE
Synonyms: 1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE;(3E)-3-[(4-chlorophenyl)imino]-1-[(4-chlorophenyl)methyl]-2,3-dihydro-1H-indol-2-one
CAS NO:478031-79-7
Molecular Formula: C21H14Cl2N2O
Molecular Weight: 381.25
EINECS: N/A
Product Categories: N/A
Mol File: 478031-79-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(478031-79-7)
EPA Substance Registry System: 1-(4-CHLOROBENZYL)-3-[(4-CHLOROPHENYL)IMINO]-1,3-DIHYDRO-2H-INDOL-2-ONE(478031-79-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 478031-79-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 478031-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,3 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 478031-79:
(8*4)+(7*7)+(6*8)+(5*0)+(4*3)+(3*1)+(2*7)+(1*9)=167
167 % 10 = 7
So 478031-79-7 is a valid CAS Registry Number.

478031-79-7Upstream product

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478031-79-7Relevant academic research and scientific papers

Solvent free synthesis of N-alkylated imino indoline-2-one derivatives under microwave irradiation

Zekavati, Roya,Doulah, Abdolhasan,Mohammadi, Mohammad Kazem,Shirali, Saloomeh

, p. 393 - 398 (2018)

The solvent-free microwave-assisted syntheses of N-alkyl isatin Schiff base derivatives are reported. These isatin derivatives are obtained as a result of the condensation of an isatin compound with a benzyl halide and an aniline derivatives using microwave irradiation condition in high yield and short reaction time.

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