Cas 892239-72-4,3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione

892239-72-4

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Basic information

Product Name: 3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione
Synonyms: 3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione
CAS NO:892239-72-4
Molecular Formula:
Molecular Weight: 471.503
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: 3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione(892239-72-4)
EPA Substance Registry System: 3-(1,3-benzothiazol-2-ylamino)-6,6-dimethyl-1-phenyl-3-trifluoromethyl-3,5,6,7-tetrahydro-1H-indole-2,4-dione(892239-72-4)

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: 892239-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 892239-72-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,2,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 892239-72:
(8*8)+(7*9)+(6*2)+(5*2)+(4*3)+(3*9)+(2*7)+(1*2)=204
204 % 10 = 4
So 892239-72-4 is a valid CAS Registry Number.

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892239-72-4Relevant academic research and scientific papers

Cyclocondensation of methyl 2-(1,3-benzothiazol-2-ylimino)-3,3,3- trifluoropropionate with C,N-binucleophiles

Sokolov,Aksinenko

, p. 934 - 936 (2011)

Reactions of methyl 2-(1,3-benzothiazol-2-ylimino)-3,3,3- trifluoropropionate with 1,3-C,N-binucleophiles, methyl 2-aminobut-2-enoate, 2-aminobut-2-enenitrile and N-substituted 6-aminouracils and 3-aminocyclohex-2-en-1-ones, led to the formation of triflu

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