Cas 426823-96-3,1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one

426823-96-3

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Basic information

Product Name: 1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one
Synonyms: 1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one
CAS NO:426823-96-3
Molecular Formula:
Molecular Weight: 487.176
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: 1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one(426823-96-3)
EPA Substance Registry System: 1-(2-chloro-5-trifluoromethyl-phenyl)-2,6,6-trimethyl-3-(2,2,2-trichloro-ethyl)-1,5,6,7-tetrahydro-indol-4-one(426823-96-3)

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: 426823-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 426823-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,8,2 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 426823-96:
(8*4)+(7*2)+(6*6)+(5*8)+(4*2)+(3*3)+(2*9)+(1*6)=163
163 % 10 = 3
So 426823-96-3 is a valid CAS Registry Number.

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426823-96-3Relevant academic research and scientific papers

A new method for the synthesis of N-substituted (4-oxo-4,5,6,7-tetrahydroindol-3-yl)acetic acids

Dudinov,Kozhinov,Krayushkin

, p. 1259 - 1263 (2007/10/03)

A new method for the synthesis of N-substituted 2-(4-oxo-4,5,6,7-tetrahydroindol-3-yl)acetic acids was developed. Alkylation of cyclic 1,3-diketones with 3,5,5,5-tetrachloropentan-2-one affords 1,4-diketones, which undergo cyclization with different primary amines into N-substituted 3-(2,2,2-trichloroethyl)-4,5,6,7-tetrahydroindol-4-ones. Acid hydrolysis of the latter gives the corresponding indol-3-ylacetic acids. The structures of the compounds obtained were confirmed by 1H and 13C NMR data.

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