Cas 452977-10-5,tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate

452977-10-5

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Basic information

Product Name: tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate
Synonyms: tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate
CAS NO:452977-10-5
Molecular Formula:
Molecular Weight: 372.381
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: tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate(452977-10-5)
EPA Substance Registry System: tert-butyl N-{(1S)-1-[(3R,3aR,6aS)-perhydrofuro[2,3-b]furan-3-yl]-2-[(4S)-4-benzyl-2-oxo-1,3-oxazolan-3-yl]-2-oxoethyl}carbamate(452977-10-5)

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: 452977-10-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 452977-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,2,9,7 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 452977-10:
(8*4)+(7*5)+(6*2)+(5*9)+(4*7)+(3*7)+(2*1)+(1*0)=175
175 % 10 = 5
So 452977-10-5 is a valid CAS Registry Number.

452977-10-5Upstream product

90719-32-7 (S)-4-Benzyl-2-oxazolidinone

452977-10-5Downstream Products

452977-10-5Relevant academic research and scientific papers

Synthesis of novel amino acids, L-bis-tetrahydrofuranylglycines

Ami, Ei'Ichi,Rajesh,Wang, Jung,Kimura, Tooru,Hayashi, Yoshio,Kiso, Yoshiaki,Ishida, Toshimasa

, p. 2931 - 2934 (2007/10/03)

Novel amino acids, enantiomerically pure L-bis-tetrahydrofuranylglycines, were efficiently synthesized from dihydrofuran utilizing radical cyclization and chiral azidation as the key steps. The absolute stereochemistry of both diastereomers has been ascertained by their crystal structures.

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