Cas 675624-13-2,(1S,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine

675624-13-2

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Basic information

Product Name: (1S,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine
Synonyms: (1S,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine
CAS NO:675624-13-2
Molecular Formula:
Molecular Weight: 297.395
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,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine(675624-13-2)
EPA Substance Registry System: (1S,2R,5R,8R,8aR)-5-[2'-oxo-2'-(cyclohexyl)ethyl]-1,2,8-trihydroxy-indolizidine(675624-13-2)

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: 675624-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 675624-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,6,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 675624-13:
(8*6)+(7*7)+(6*5)+(5*6)+(4*2)+(3*4)+(2*1)+(1*3)=182
182 % 10 = 2
So 675624-13-2 is a valid CAS Registry Number.

675624-13-2Upstream product

675624-13-2Downstream Products

675624-13-2Relevant academic research and scientific papers

Synthesis of the new mannosidase inhibitors, diversity-oriented 5-substituted swainsonine analogues, via stereoselective mannich reaction

Fujita, Tomoya,Nagasawa, Hideko,Uto, Yoshihiro,Hashimoto, Toshihiro,Asakawa, Yoshinori,Hori, Hitoshi

, p. 827 - 830 (2007/10/03)

5α-Substituted swainsonine analogues were synthesized by Mannich reaction of an in situ generated (-)-swainsonine iminium ion intermediate. 5α-Substituted swainsonine analogues were epimerized to their 5β-isomers in protic solvent.

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