Cas 1105065-59-5,tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate

1105065-59-5

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Basic information

Product Name: tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate
Synonyms: tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate
CAS NO:1105065-59-5
Molecular Formula:
Molecular Weight: 378.536
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: tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate(1105065-59-5)
EPA Substance Registry System: tert-butyl (2S,3S,R(S))-[2-cyano-5-methyl-1-(p-tolylsulfinyl)hexan-3-yl]carbamate(1105065-59-5)

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: 1105065-59-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1105065-59-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,5,0,6 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1105065-59:
(9*1)+(8*1)+(7*0)+(6*5)+(5*0)+(4*6)+(3*5)+(2*5)+(1*9)=105
105 % 10 = 5
So 1105065-59-5 is a valid CAS Registry Number.

1105065-59-5Upstream product

1105065-59-5Downstream Products

1105065-59-5Relevant academic research and scientific papers

γ-Amino vinyl sulfoxides in asymmetric synthesis. Synthesis of optically pure α-substituted β-amino nitriles

Alfaro, Ricardo,Yuste, Francisco,Ortiz, Benjamín,Sánchez-Obregón, Rubén,García Ruano, José L.

, p. 357 - 363 (2009)

The synthesis of optically pure (E)- and (Z)-γ-amino vinyl sulfoxides derived from commercially available protected α-amino esters is reported. Hydrocyanation of the double bond with Et2AlCN is completely stereoselective and provides enantiomer

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