Cas 1010691-49-2,(S)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine

1010691-49-2

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Basic information

Product Name: (S)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine
Synonyms: (S)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine
CAS NO:1010691-49-2
Molecular Formula:
Molecular Weight: 398.569
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)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine(1010691-49-2)
EPA Substance Registry System: (S)-N-[2-[(4S)-4-(tert-butyl)-4,5-dihydro-2-oxazolyl]phenyl]-S-(iso-butyl)-S-phenylsulfoximine(1010691-49-2)

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: 1010691-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1010691-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,6,9 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1010691-49:
(9*1)+(8*0)+(7*1)+(6*0)+(5*6)+(4*9)+(3*1)+(2*4)+(1*9)=102
102 % 10 = 2
So 1010691-49-2 is a valid CAS Registry Number.

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1010691-49-2Relevant academic research and scientific papers

C1-symmetric oxazolinyl sulfoximines as ligands in copper-catalyzed asymmetric mukaiyama aldol reactions

Sedelmeier, Joerg,Hammerer, Tim,Bolm, Carsten

supporting information; experimental part, p. 917 - 920 (2009/04/07)

Aryl-bridged C1-symmetric oxazolinyl sulfoximines are applicable in copper-catalyzed asymmetric Mukaiyama aldol reactions with methyl pyruvate. The resulting a-hydroxy esters have been obtained with up to 94% ee in good yields. They contain a quaternary stereogenic center and represent valuable precursors for biologically active molecules.

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