Cas 109417-64-3,(S)-(+)-N-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine

109417-64-3

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Basic information

Product Name: (S)-(+)-N-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine
Synonyms: (S)-(+)-N-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine
CAS NO:109417-64-3
Molecular Formula:
Molecular Weight: 391.488
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-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine(CAS DataBase Reference)
NIST Chemistry Reference: (S)-(+)-N-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine(109417-64-3)
EPA Substance Registry System: (S)-(+)-N-ethoxycarbonylmethyl-S-o-(2-methoxyethoxy)phenyl-S-p-tolylsulfoximine(109417-64-3)

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: 109417-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109417-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,1 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109417-64:
(8*1)+(7*0)+(6*9)+(5*4)+(4*1)+(3*7)+(2*6)+(1*4)=123
123 % 10 = 3
So 109417-64-3 is a valid CAS Registry Number.

109417-64-3Upstream product

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109417-64-3Relevant academic research and scientific papers

Chiral Induction in the Methylation of N-Ethoxycarbonylmethyl Sulfoximines

Hambley, Trevor W.,Raguse, Burkhard,Ridley, Damon D.

, p. 1833 - 1842 (2007/10/02)

Chiral inductions in the C-methylations of four optically active N-ethoxycarbonylmethyl-S-p-tolylsulfoximines were explored by using the reagents lithium diisopropylamide (in tetrahydrofuran at -78 deg) then methyl iodide.When the fourth substituent at su

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