Cas 1357445-10-3,(S,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine

1357445-10-3

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Basic information

Product Name: (S,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine
Synonyms: (S,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine
CAS NO:1357445-10-3
Molecular Formula:
Molecular Weight: 357.433
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,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine(CAS DataBase Reference)
NIST Chemistry Reference: (S,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine(1357445-10-3)
EPA Substance Registry System: (S,E)-(-)-N'-((4-acetamidophenyl)sulfinyl)-N,N-dimethyl-2-oxo-2-phenylacetamidine(1357445-10-3)

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: 1357445-10-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357445-10-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,4,4 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1357445-10:
(9*1)+(8*3)+(7*5)+(6*7)+(5*4)+(4*4)+(3*5)+(2*1)+(1*0)=163
163 % 10 = 3
So 1357445-10-3 is a valid CAS Registry Number.

1357445-10-3Upstream product

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1357445-10-3Relevant academic research and scientific papers

Rhodium(II)-catalyzed asymmetric sulfur(VI) reduction of diazo sulfonylamidines

Selander, Nicklas,Fokin, Valery V.

, p. 2477 - 2480 (2012/04/04)

Diazo sulfonylamidines readily undergo enantioselective oxygen transfer from sulfur to carbon atom in the presence of chiral rhodium(II) carboxylates resulting in chiral sulfinylamidines. This unusual asymmetric atom transfer "reduction" occurs rapidly under mild conditions, and sulfinylamidines are obtained in excellent yield.

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