Cas 1609490-95-0,(S<SUB>s</SUB>,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate

1609490-95-0

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Basic information

Product Name: (S_s,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate
Synonyms: (S_s,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate
CAS NO:1609490-95-0
Molecular Formula:
Molecular Weight: 419.927
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_s,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S_s,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate(1609490-95-0)
EPA Substance Registry System: (S_s,2S,3S)-ethyl 2-(tert-butoxycarbonyloxy)-4-chloro-3-(p-toluenesulfinylamino)butanoate(1609490-95-0)

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: 1609490-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609490-95-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,9 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1609490-95:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*9)+(3*0)+(2*9)+(1*5)=190
190 % 10 = 0
So 1609490-95-0 is a valid CAS Registry Number.

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1609490-95-0Relevant academic research and scientific papers

Asymmetric synthesis of chloroisothreonine derivatives via syn-stereoselective Mannich-type additions across N-sulfinyl-α- chloroimines

Callebaut, Gert,Colpaert, Filip,Nonn, Melinda,Kiss, Lorand,Sillanpaeae, Reijo,Toernroos, Karl W.,Fueloep, Ferenc,De Kimpe, Norbert,Mangelinckx, Sven

, p. 3393 - 3405 (2014/05/20)

Mannich-type reactions of O-Boc glycolic esters across chiral N-sulfinyl-α-chloroaldimines resulted in the efficient and syn-stereoselective synthesis of new γ-chloro-α-hydroxy-β-amino esters (dr > 99 : 1). The α-coordinating ability of the chlorine atom

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