Cas 1377574-63-4,(E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene

1377574-63-4

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Basic information

Product Name: (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene
Synonyms: (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene
CAS NO:1377574-63-4
Molecular Formula:
Molecular Weight: 487.598
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: (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene(1377574-63-4)
EPA Substance Registry System: (E)-2-(1-(4-methoxyphenyl)-3-(4-nitrophenyl)allyl)-6-methyl-3-p-tolyl-1H-indene(1377574-63-4)

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: 1377574-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1377574-63-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,7,5,7 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1377574-63:
(9*1)+(8*3)+(7*7)+(6*7)+(5*5)+(4*7)+(3*4)+(2*6)+(1*3)=204
204 % 10 = 4
So 1377574-63-4 is a valid CAS Registry Number.

1377574-63-4Upstream product

1377574-63-4Downstream Products

1377574-63-4Relevant academic research and scientific papers

Carbon-carbon bond formation via the electrophilic addition of carbocations to allenes

Meng, Bo,Ma, Shengming

supporting information; experimental part, p. 2674 - 2677 (2012/07/14)

A novel electrophilic addition of aryl-substituted allenes and carbocations forming a carbon-carbon bond is described. Stereodefined allylic halides and indenes were furnished with excellent regio- and stereoselectivity depending on the structure of allenes.

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