Cas 1602487-68-2,(E)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide

1602487-68-2

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Basic information

Product Name: (E)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide
Synonyms: (E)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide
CAS NO:1602487-68-2
Molecular Formula:
Molecular Weight: 361.912
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)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide(1602487-68-2)
EPA Substance Registry System: (E)-3-(4-chlorophenyl)-N-(2-((1R,2R,4S)-2-hydroxy-1,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)ethyl)acrylamide(1602487-68-2)

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: 1602487-68-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1602487-68-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,2,4,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1602487-68:
(9*1)+(8*6)+(7*0)+(6*2)+(5*4)+(4*8)+(3*7)+(2*6)+(1*8)=162
162 % 10 = 2
So 1602487-68-2 is a valid CAS Registry Number.

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1602487-68-2Relevant academic research and scientific papers

Enantiopure antituberculosis candidates synthesized from (-)-fenchone

Dobrikov, Georgi M.,Valcheva, Violeta,Nikolova, Yana,Ugrinova, Iva,Pasheva, Evdokia,Dimitrov, Vladimir

supporting information, p. 243 - 247 (2014/04/03)

The synthesis of new enantiopure N-acyl compounds derived from (-)-fenchone has been performed. The evaluation of their in vitro activity against Mycobacterium tuberculosis H37Rv showed for most of them moderate activity. The structures bearing

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