Cas 179077-89-5,(1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol

179077-89-5

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Basic information

Product Name: (1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol
Synonyms: (1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol
CAS NO:179077-89-5
Molecular Formula:
Molecular Weight: 360.564
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: (1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(179077-89-5)
EPA Substance Registry System: (1S,2S,5S)-3-[(E)-(R)-2-Cyclohexyl-1-thiazol-2-yl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(179077-89-5)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 179077-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179077-89-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,7 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 179077-89:
(8*1)+(7*7)+(6*9)+(5*0)+(4*7)+(3*7)+(2*8)+(1*9)=185
185 % 10 = 5
So 179077-89-5 is a valid CAS Registry Number.

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179077-89-5Relevant academic research and scientific papers

Alkylation of camphor and pinanone imines of 2-(aminomethyl)thiazole. Enantioselective synthesis of 2-(1-aminoalkyl)thiazoles

Dondoni, Alessandro,Merchan, Francisco L.,Merino, Pedro,Rojo, Isabel,Tejero, Tomas

, p. 641 - 646 (1996)

A method is described for the enantioselective synthesis of 2-(1-aminoalkyl)thiazoles 6 via stereoselective alkylation of the carbanions of (+)-(R)-camphor and (-)-(1S, 2S, 5S)-2-hydroxypinan-3-one imines 2 and 3 derived from 2-(aminomethyl)thiazole (2-AMT, 1). Compounds 6 serve as α-amino aldehyde precursors via thiazolyl-to-formyl conversion.

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