Cas 127612-47-9,2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol

127612-47-9

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Basic information

Product Name: 2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol
Synonyms: 2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol
CAS NO:127612-47-9
Molecular Formula:
Molecular Weight: 715.481
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: 2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol(127612-47-9)
EPA Substance Registry System: 2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol(127612-47-9)

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: 127612-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127612-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,1 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127612-47:
(8*1)+(7*2)+(6*7)+(5*6)+(4*1)+(3*2)+(2*4)+(1*7)=119
119 % 10 = 9
So 127612-47-9 is a valid CAS Registry Number.

127612-47-9Upstream product

127612-47-9Downstream Products

127612-47-9Relevant academic research and scientific papers

A UNIQUE TRIMOLECULAR MICHAEL REACTION AND CYCLIZATION

Al-Arab, Mohamed M.,Ghanem, Bader S.,Fitton, Alan O.

, p. 6545 - 6552 (1989)

1,3-Diaryl-2-propene-1-ones react with ethyl cyanoacetate in presence of sodium ethoxide at room temperature to give 2-aroyl-1,3,5-triaryl-4-carbethoxy-4-cyanocyclohexanols.The structure of the reaction products was established by infrared, H-1 and C-13 n

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