Cas 332048-56-3,(+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide

332048-56-3

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Basic information

Product Name: (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide
Synonyms: (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide
CAS NO:332048-56-3
Molecular Formula:
Molecular Weight: 512.692
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: (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide(CAS DataBase Reference)
NIST Chemistry Reference: (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide(332048-56-3)
EPA Substance Registry System: (+)-2-(2-(N,N'-bis(t-butoxycarbonyl)hydrazino)-2-phenylethanoyl)-2-(R)-ethyl-1,3-dithiane 1-(R)-oxide(332048-56-3)

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: 332048-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 332048-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,0,4 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 332048-56:
(8*3)+(7*3)+(6*2)+(5*0)+(4*4)+(3*8)+(2*5)+(1*6)=113
113 % 10 = 3
So 332048-56-3 is a valid CAS Registry Number.

332048-56-3Upstream product

332048-56-3Downstream Products

332048-56-3Relevant academic research and scientific papers

Electrophilic amination of ketone enolates mediated by the DiTOX asymmetric building block: Enantioselective formal synthesis of α-aminoacids

Bulman Page, Philip C.,McKenzie, Michael J.,Allin, Steven M.,Buckle, Derek R.

, p. 9683 - 9695 (2007/10/03)

Diastereoselective electrophilic amination of enolates derived from 2-acyl-1,3-dithiane 1-oxides is used as the key step for an enantioselective synthesis of two α-hydrazido carboxylic acids, well-known precursors of α-amino acids. (C) 2000 Elsevier Science Ltd.

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