Cas 200623-13-8,{(S)-2-[(2S,4R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidin-1-yl]-1-methyl-2-oxo-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester

200623-13-8

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Basic information

Product Name: {(S)-2-[(2S,4R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidin-1-yl]-1-methyl-2-oxo-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester
Synonyms:
CAS NO:200623-13-8
Molecular Formula:
Molecular Weight: 951.247
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: {(S)-2-[(2S,4R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidin-1-yl]-1-methyl-2-oxo-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(S)-2-[(2S,4R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidin-1-yl]-1-methyl-2-oxo-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(200623-13-8)
EPA Substance Registry System: {(S)-2-[(2S,4R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-diphenyl-silanyloxy)-pyrrolidin-1-yl]-1-methyl-2-oxo-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(200623-13-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 200623-13-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 200623-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,6,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 200623-13:
(8*2)+(7*0)+(6*0)+(5*6)+(4*2)+(3*3)+(2*1)+(1*3)=68
68 % 10 = 8
So 200623-13-8 is a valid CAS Registry Number.

200623-13-8Upstream product

200623-13-8Downstream Products

200623-13-8Relevant academic research and scientific papers

The solid phase synthesis of trisubstituted 1,4-diazabicyclo[4.3.0]nonan-2-one scaffolds: On bead monitoring of heterocycle forming reactions using 15N NMR

Swayze, Eric E.

, p. 8643 - 8646 (1997)

Several representative 3,4,8-trisubstituted 1,4-diazabicyclo[3.4.0]nonan-2-ones have been prepared employing solid phase methodologies. Elaboration of a 4-hydroxyproline derivative with an 15N-amino acid derivative allowed convenient monitoring of the reaction sequence on solid support by gel-phase 15N NMR. An intramolecular Mitsunobu cyclization provided the desired heterocycle, which could be further functionalized at the 4-position. This synthetic method is facile, general, and suitable for the construction of large libraries of compounds for biological assays.

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