Cas 944055-61-2,3-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one

944055-61-2

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Basic information

Product Name: 3-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one
Synonyms: 3-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one
CAS NO:944055-61-2
Molecular Formula:
Molecular Weight: 478.427
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-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one(944055-61-2)
EPA Substance Registry System: 3-[(2-methyl-4-nitroindol-3-yl)-o-(trifluoromethyl)phenylmethyl]-4H-chromen-4-one(944055-61-2)

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: 944055-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 944055-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,0,5 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 944055-61:
(8*9)+(7*4)+(6*4)+(5*0)+(4*5)+(3*5)+(2*6)+(1*1)=172
172 % 10 = 2
So 944055-61-2 is a valid CAS Registry Number.

944055-61-2Upstream product

944055-61-2Downstream Products

944055-61-2Relevant academic research and scientific papers

A highly α-regioselective AgOTf-catalyzed nucleophilic substitution of the Baylis-Hillman acetates with indoles

Shafiq, Zahid,Liu, Li,Liu, Zhe,Wang, Dong,Chen, Yong-Jun

, p. 2525 - 2528 (2008/02/05)

An efficient method for highly α-regioselective nucleophillc substitution of the Baylis-Hillman acetates with Indoles catalyzed by AgOTf in high yields (72-99%) has been developed. Reductive cyclization of the substitution products furnished the azepinoin

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