Cas 1333261-91-8,(3S,3aS,4R,5R,6aS)-ethyl 5-(benzylamino)-6a-(tert-butoxycarbonylamino)-3a-hydroxy-3-isopropyl-1-oxooctahydrocyclopenta[c]pyrrole-4-carboxylate

1333261-91-8

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Basic information

Product Name: (3S,3aS,4R,5R,6aS)-ethyl 5-(benzylamino)-6a-(tert-butoxycarbonylamino)-3a-hydroxy-3-isopropyl-1-oxooctahydrocyclopenta[c]pyrrole-4-carboxylate
Synonyms:
CAS NO:1333261-91-8
Molecular Formula:
Molecular Weight: 475.585
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: (3S,3aS,4R,5R,6aS)-ethyl 5-(benzylamino)-6a-(tert-butoxycarbonylamino)-3a-hydroxy-3-isopropyl-1-oxooctahydrocyclopenta[c]pyrrole-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,3aS,4R,5R,6aS)-ethyl 5-(benzylamino)-6a-(tert-butoxycarbonylamino)-3a-hydroxy-3-isopropyl-1-oxooctahydrocyclopenta[c]pyrrole-4-carboxylate(1333261-91-8)
EPA Substance Registry System: (3S,3aS,4R,5R,6aS)-ethyl 5-(benzylamino)-6a-(tert-butoxycarbonylamino)-3a-hydroxy-3-isopropyl-1-oxooctahydrocyclopenta[c]pyrrole-4-carboxylate(1333261-91-8)

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: 1333261-91-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333261-91-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,6 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1333261-91:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*6)+(3*1)+(2*9)+(1*1)=128
128 % 10 = 8
So 1333261-91-8 is a valid CAS Registry Number.

1333261-91-8Upstream product

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1333261-91-8Relevant academic research and scientific papers

Concise pathway to new multifunctionalized constrained pentacin derivatives by means of two stereospecific tandem reactions

Coursindel, Thibault,Martinez, Jean,Parrot, Isabelle

, p. 4519 - 4522 (2011)

Starting from Boc-activated diketopiperazines, original bicyclic derivatives of trans-and cis-2-aminocyclopentane carboxylic acid were prepared by using two stereospecific tandem reactions. One of them is a tandem transannular rearrangement of activated lactams/alkylation process leading to the stereoselective synthesis of suitably chiral pyrrolidine-2, 4-diones, allowing subsequent Michael-initiated ring closure, a simple and concise route to original multifunctionalized alicyclic ss-amino esters.

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