Cas 1253233-11-2,(2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate

1253233-11-2

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Basic information

Product Name: (2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate
Synonyms: (2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate
CAS NO:1253233-11-2
Molecular Formula:
Molecular Weight: 515.784
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: (2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate(1253233-11-2)
EPA Substance Registry System: (2S,3S,αS)-tert-butyl 5-(tert-butyldimethylsilyloxy)-3-(N-benzyl-α-methylbenzylamino)-2-fluoropentanoate(1253233-11-2)

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: 1253233-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1253233-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,3,2,3 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1253233-11:
(9*1)+(8*2)+(7*5)+(6*3)+(5*2)+(4*3)+(3*3)+(2*1)+(1*1)=112
112 % 10 = 2
So 1253233-11-2 is a valid CAS Registry Number.

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1253233-11-2Relevant academic research and scientific papers

Enantioselective synthesis of α-fluoro-β3-amino esters: Synthesis of enantiopure, orthogonally protected α-fluoro- β3-lysine

Duggan, Peter J.,Johnston, Martin,March, Taryn L.

experimental part, p. 7365 - 7372 (2011/02/23)

The scope of a tandem conjugate addition-fluorination sequence performed on α,β-unsaturated esters using the enantiopure lithium amide derived from (S)-N-benzyl-N-(α-methylbenzyl)amine, and the electrophilic fluorinating agent N-fluorobenzenesulfonimide h

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