Cas 1383535-35-0,5-chloro-2-{2-methyl-4-[1-(4-nitrobenzenesulfonyl)-2-oxo-5-trifluoromethoxy-1,2-dihydro-indol-3-ylideneamino]phenyl}isoindole-1,3-dione

1383535-35-0

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Basic information

Product Name: 5-chloro-2-{2-methyl-4-[1-(4-nitrobenzenesulfonyl)-2-oxo-5-trifluoromethoxy-1,2-dihydro-indol-3-ylideneamino]phenyl}isoindole-1,3-dione
Synonyms:
CAS NO:1383535-35-0
Molecular Formula:
Molecular Weight: 684.993
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-chloro-2-{2-methyl-4-[1-(4-nitrobenzenesulfonyl)-2-oxo-5-trifluoromethoxy-1,2-dihydro-indol-3-ylideneamino]phenyl}isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-chloro-2-{2-methyl-4-[1-(4-nitrobenzenesulfonyl)-2-oxo-5-trifluoromethoxy-1,2-dihydro-indol-3-ylideneamino]phenyl}isoindole-1,3-dione(1383535-35-0)
EPA Substance Registry System: 5-chloro-2-{2-methyl-4-[1-(4-nitrobenzenesulfonyl)-2-oxo-5-trifluoromethoxy-1,2-dihydro-indol-3-ylideneamino]phenyl}isoindole-1,3-dione(1383535-35-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1383535-35-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1383535-35-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,5,3 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1383535-35:
(9*1)+(8*3)+(7*8)+(6*3)+(5*5)+(4*3)+(3*5)+(2*3)+(1*5)=170
170 % 10 = 0
So 1383535-35-0 is a valid CAS Registry Number.

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1383535-35-0Relevant academic research and scientific papers

Synthesis and in vitro antibacterial activity of schiff bases of N-substituted isatins as effective scaffolds

Kumari, Garima,Singh, Ramendra K.

, p. 927 - 933 (2013)

Novel Schiff bases of N-substituted isatin, 1-13, were synthesized starting from isatin and N-(4-amino-2-methylphenyl)-4-chlorophthalimide and their structures were confirmed by spectral and elemental analyses. All new compounds were tested for their in v

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