Cas 911381-63-0,(-)-[S<sub>S</sub>,N(1S)]-N-{1-[tert-butyl(dimethyl)silanyloxymethyl]-2-methyl-propyl}-1-benzyl-3-(p-tolyl-sulfonimidomethyl)-2,5-dihydro-1H-pyrrole

911381-63-0

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Basic information

Product Name: (-)-[S_S,N(1S)]-N-{1-[tert-butyl(dimethyl)silanyloxymethyl]-2-methyl-propyl}-1-benzyl-3-(p-tolyl-sulfonimidomethyl)-2,5-dihydro-1H-pyrrole
Synonyms:
CAS NO:911381-63-0
Molecular Formula:
Molecular Weight: 526.859
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,N(1S)]-N-{1-[tert-butyl(dimethyl)silanyloxymethyl]-2-methyl-propyl}-1-benzyl-3-(p-tolyl-sulfonimidomethyl)-2,5-dihydro-1H-pyrrole(CAS DataBase Reference)
NIST Chemistry Reference: (-)-[S_S,N(1S)]-N-{1-[tert-butyl(dimethyl)silanyloxymethyl]-2-methyl-propyl}-1-benzyl-3-(p-tolyl-sulfonimidomethyl)-2,5-dihydro-1H-pyrrole(911381-63-0)
EPA Substance Registry System: (-)-[S_S,N(1S)]-N-{1-[tert-butyl(dimethyl)silanyloxymethyl]-2-methyl-propyl}-1-benzyl-3-(p-tolyl-sulfonimidomethyl)-2,5-dihydro-1H-pyrrole(911381-63-0)

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: 911381-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 911381-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,3,8 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 911381-63:
(8*9)+(7*1)+(6*1)+(5*3)+(4*8)+(3*1)+(2*6)+(1*3)=150
150 % 10 = 0
So 911381-63-0 is a valid CAS Registry Number.

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911381-63-0Relevant academic research and scientific papers

Synthesis of highly functionalized azabicycles via 2-alkenyl sulfoximines

Reggelin, Michael,Kuehl, Jochen,Kaiser, Jan Philipp,Buehle, Philipp

, p. 2224 - 2232 (2008/02/02)

Functionalized cycloalkanones have been converted into enantiomerically pure endocyclic 2-alkenyl sulfoximines. Titanated derivatives thereof undergo highly diastereoselective γ-hydroxyalkylation reactions with various amino aldehydes yielding isomerically pure vinyl sulfoximines, which can be cyclized by N-deprotection. The resulting heterobicyclic systems are expected to be interesting scaffolds for the synthesis of topological mimetics of peptides. Georg Thieme Verlag Stuttgart.

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