Cas 1579298-94-4,(3-(3,5-bis(trifluoromethyl)phenylimino)-1-butylindolin-2-ylidene)-3,5-bis(trifluoromethyl)benzenamine

1579298-94-4

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Basic information

Product Name: (3-(3,5-bis(trifluoromethyl)phenylimino)-1-butylindolin-2-ylidene)-3,5-bis(trifluoromethyl)benzenamine
Synonyms:
CAS NO:1579298-94-4
Molecular Formula:
Molecular Weight: 625.46
EINECS: N/A
Product Categories: N/A
Mol File: 1579298-94-4.mol
Article Data: 1

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-(3,5-bis(trifluoromethyl)phenylimino)-1-butylindolin-2-ylidene)-3,5-bis(trifluoromethyl)benzenamine(CAS DataBase Reference)
NIST Chemistry Reference: (3-(3,5-bis(trifluoromethyl)phenylimino)-1-butylindolin-2-ylidene)-3,5-bis(trifluoromethyl)benzenamine(1579298-94-4)
EPA Substance Registry System: (3-(3,5-bis(trifluoromethyl)phenylimino)-1-butylindolin-2-ylidene)-3,5-bis(trifluoromethyl)benzenamine(1579298-94-4)

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: 1579298-94-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1579298-94-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,2,9 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1579298-94:
(9*1)+(8*5)+(7*7)+(6*9)+(5*2)+(4*9)+(3*8)+(2*9)+(1*4)=244
244 % 10 = 4
So 1579298-94-4 is a valid CAS Registry Number.

1579298-94-4Upstream product

22014-99-9 N-butylindole

1579298-94-4Downstream Products

1579298-94-4Relevant articles and documents

Ruthenium porphyrin catalyzed diimination of indoles with aryl azides as the nitrene source

Wei, Jinhu,Xiao, Wenbo,Zhou, Cong-Ying,Che, Chi-Ming

supporting information, p. 3373 - 3376 (2014/03/21)

By using [Ru(TTP)CO] [H2TTP = meso-tetrakis(4-tolyl)porphyrin] as catalyst and aryl azides as the nitrene source, the sp2(C-H) bonds of a series of indoles undergo oxidative C-N bond formation to give unique 2,3-diimination products in good to high yields. The Royal Society of Chemistry 2014.

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