Cas 147976-11-2,(S)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one

147976-11-2

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Basic information

Product Name: (S)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one
Synonyms: (S)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one
CAS NO:147976-11-2
Molecular Formula:
Molecular Weight: 496.403
EINECS: N/A
Product Categories: N/A
Mol File: 147976-11-2.mol
Article Data: 1

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)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one(147976-11-2)
EPA Substance Registry System: (S)-3-(9-phenylfluoren-9-yl)-4-<(2-bromophenyl)methyl>oxazolidin-5-one(147976-11-2)

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: 147976-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147976-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,9,7 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 147976-11:
(8*1)+(7*4)+(6*7)+(5*9)+(4*7)+(3*6)+(2*1)+(1*1)=172
172 % 10 = 2
So 147976-11-2 is a valid CAS Registry Number.

147976-11-2Upstream product

147976-11-2Downstream Products

147976-11-2Relevant articles and documents

Synthesis of 2--1-indanones by Anionic Cyclization of Phenylalanine-Derived Oxazolidinones

Paleo, M. Rita,Castedo, Luis,Dominguez, Domingo

, p. 2763 - 2767 (2007/10/02)

A novel preparation of N-(phenylfluorenyl)-2-amino-1-indanones is described.The key step is the cyclization of aryl-substituted o-bromophenylalanine-derived oxazolidinones with n-BuLi by halogen-metal exchange followed by in situ intramolecular acylation

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