Cas 926643-72-3,(7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one

926643-72-3

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Basic information

Product Name: (7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one
Synonyms: (7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one
CAS NO:926643-72-3
Molecular Formula:
Molecular Weight: 273.375
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: (7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one(926643-72-3)
EPA Substance Registry System: (7S,8R,8aS)-8-benzyloxy-7-ethyl-1,2,3,5,6,7,8,8a-octahydroindolizin-3-one(926643-72-3)

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: 926643-72-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 926643-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,6,4 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 926643-72:
(8*9)+(7*2)+(6*6)+(5*6)+(4*4)+(3*3)+(2*7)+(1*2)=193
193 % 10 = 3
So 926643-72-3 is a valid CAS Registry Number.

926643-72-3Upstream product

100-39-0 benzyl bromide

926643-72-3Downstream Products

926643-73-4 8-benzyloxy-7-ethyl-octahydro-indolizine

926643-72-3Relevant academic research and scientific papers

An expedient synthesis of 7(S)-ethyl-8(R or S)-indolizidinols based on a thiophene reductive desulfurization

Marchalín, ?tefan,?ú?iová, Jozefína,Kadle?íková, Katarína,?afá?, Peter,Baran, Peter,Dalla, Vincent,Da?ch, Adam

, p. 697 - 702 (2007)

Chiral hexahydrothieno[2,3-f]indolizine-4,7-dione (S)-12 and the ancillary alcohol 13 were generated from thiophene-2-carboxaldehyde and (S)-glutamic acid in three and four steps, respectively, in good overall yields and both high enantio- and diastereome

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