Cas 142013-03-4,Fluoro-(4-methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester

142013-03-4

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Basic information

Product Name: Fluoro-(4-methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester
Synonyms:
CAS NO:142013-03-4
Molecular Formula:
Molecular Weight: 455.591
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: Fluoro-(4-methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Fluoro-(4-methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(142013-03-4)
EPA Substance Registry System: Fluoro-(4-methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester(142013-03-4)

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: 142013-03-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 142013-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,1 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142013-03:
(8*1)+(7*4)+(6*2)+(5*0)+(4*1)+(3*3)+(2*0)+(1*3)=64
64 % 10 = 4
So 142013-03-4 is a valid CAS Registry Number.

142013-03-4Upstream product

130517-53-2 (4-Methoxy-phenyl)-acetic acid (1S,2R,4R)-1-diethylsulfamoylmethyl-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester

142013-03-4Downstream Products

142013-03-4Relevant academic research and scientific papers

Diastereoselective fluorination at benzyl position by anodic oxidation

Kabore,Chebli,Faure,Laurent,Marquet

, p. 3137 - 3140 (1990)

By anodic oxidation of benzylic derivatives 1 in Et3N,3HF/CH3CN, diastereoselective fluorination in the α position of the electron withdrawing group is obtained. The observed stereoselectivities are discussed in connection with the i

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