Cas 284677-00-5,(3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C<sub>2</sub>]azetidin-2-one

284677-00-5

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Basic information

Product Name: (3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C₂]azetidin-2-one
Synonyms: (3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C₂]azetidin-2-one
CAS NO:284677-00-5
Molecular Formula:
Molecular Weight: 385.525
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: (3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C₂]azetidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C₂]azetidin-2-one(284677-00-5)
EPA Substance Registry System: (3R,4S)-1-benzoyl-3-(tert-butyldimethylsilanyloxy)-4-phenyl-[2,3-14C₂]azetidin-2-one(284677-00-5)

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: 284677-00-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 284677-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,4,6,7 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 284677-00:
(8*2)+(7*8)+(6*4)+(5*6)+(4*7)+(3*7)+(2*0)+(1*0)=175
175 % 10 = 5
So 284677-00-5 is a valid CAS Registry Number.

284677-00-5Upstream product

98-88-4 benzoyl chloride

284677-00-5Downstream Products

284677-00-5Relevant academic research and scientific papers

Synthesis of [14C2]Taxol: Application of (+)/(-)-[13-14C(n)]BABS, part 3

Rodriguez,Voges

, p. 169 - 176 (2000)

A multiple step stereoselective procedure was successfully applied to doubly C-14 labelled Taxol 1 in its pharmacologically essential (2R,3S)N-benzoyl-3-phenylisoserine side chain. A highly stereocontrolled aldol reaction of internally developed (+)-[sup

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