Cas 909296-45-3,(R<sub>S</sub>,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide

909296-45-3

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Basic information

Product Name: (R_S,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide
Synonyms: (R_S,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide
CAS NO:909296-45-3
Molecular Formula:
Molecular Weight: 496.695
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: (R_S,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (R_S,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide(909296-45-3)
EPA Substance Registry System: (R_S,S)-N-[3-(N-tosylamino)-1-phenyl-3-(p-methyl-phenyl)-propylidene]-tert-butanesulfinamide(909296-45-3)

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: 909296-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909296-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,2,9 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 909296-45:
(8*9)+(7*0)+(6*9)+(5*2)+(4*9)+(3*6)+(2*4)+(1*5)=203
203 % 10 = 3
So 909296-45-3 is a valid CAS Registry Number.

909296-45-3Upstream product

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909296-45-3Relevant academic research and scientific papers

Asymmetric mannich-type reaction of a chiral N-(tert-butylsulfinyl) ketimine with imines: Application to the synthesis of chiral 1,3-diamines

Zhao, Cui-Hua,Liu, Li,Wang, Dong,Chen, Yong-Jun

, p. 2977 - 2986 (2007/10/03)

Deprotonation of the chiral N-(tert-butylsulfinyl) ketimine 1 followed by trapping with imines 2 afforded the β-amino imines 3 as the Mannich-type products in high diastereoselectivities (99:1 dr). As versatile synthons chiral β-amino imines 3 could be tr

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