Cas 347161-80-2,2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester

347161-80-2

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Basic information

Product Name: 2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester
Synonyms: 2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester
CAS NO:347161-80-2
Molecular Formula:
Molecular Weight: 607.765
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: 2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester(347161-80-2)
EPA Substance Registry System: 2,7-di-tert-butyl-5-[2-(3-fluorophenyl)ethylcarbamoyl]-9,9-dimethyl-9H-xanthene-4-carboxylic acid phenyl ester(347161-80-2)

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: 347161-80-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 347161-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,1,6 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 347161-80:
(8*3)+(7*4)+(6*7)+(5*1)+(4*6)+(3*1)+(2*8)+(1*0)=142
142 % 10 = 2
So 347161-80-2 is a valid CAS Registry Number.

347161-80-2Upstream product

404-70-6 2-(3-Fluorophenyl)ethylamine

347161-80-2Downstream Products

347161-85-7 2,7-di-tert-butyl-5-(4,6-diamino-[1.3.5]triazin-2-yl)-9,9-dimethyl-9H-xanthene-4-carboxylic acid [2-(3-fluorophenyl)ethyl]amide

347161-80-2Relevant academic research and scientific papers

Model Systems for Flavoenzyme Activity. Control of Flavin Recognition via Specific Electrostatic Interactions

Goodman, Allan J.,Breinlinger, Eric C.,McIntosh, Catherine M.,Grimaldi, Lisa N.,Rotello, Vincent M.

, p. 1531 - 1534 (2007/10/03)

matrix presented A model system has been used to study the interactions of dipole-containing aromatic systems with oxidized and reduced flavin. Ab initio computational and experimental studies show that dipole orientation within the host is a critical determinant for recognition and redox behavior of the flavin guest.

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