Cas 1263766-34-2,ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate

1263766-34-2

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Basic information

Product Name: ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate
Synonyms: ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate
CAS NO:1263766-34-2
Molecular Formula:
Molecular Weight: 440.539
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: ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate(1263766-34-2)
EPA Substance Registry System: ethyl 3-(1-(2-tert-butoxycarbonylamino)phenyl)-(3-formyl-5,6,7,8-tetrahydroindolizin-8-yl)propanoate(1263766-34-2)

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: 1263766-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1263766-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,7,6 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1263766-34:
(9*1)+(8*2)+(7*6)+(6*3)+(5*7)+(4*6)+(3*6)+(2*3)+(1*4)=172
172 % 10 = 2
So 1263766-34-2 is a valid CAS Registry Number.

1263766-34-2Upstream product

1263766-34-2Downstream Products

1263766-34-2Relevant academic research and scientific papers

Synthesis of (±)-desethylrhazinal using a tandem radical addition-cyclization process

Paleo, Ehecatl,Osornio, Yazmin M.,Miranda, Luis D.

, p. 361 - 362 (2011)

The indolizidine ring system present in (±)-rhazinal, was assembled using a xanthate-based sequential intermolecular radical addition-cyclization process. The novel (±)-desethylrhazinal was prepared in seven steps in approximately 12% overall yield from 2

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