Cas 451503-21-2,(R)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide

451503-21-2

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Basic information

Product Name: (R)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide
Synonyms: (R)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide
CAS NO:451503-21-2
Molecular Formula:
Molecular Weight: 355.424
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)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide(451503-21-2)
EPA Substance Registry System: (R)-2-methyl-N-[(R)-phenyl[4-(trifluoromethyl)-phenyl]methyl]-2-propanesulfinamide(451503-21-2)

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: 451503-21-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 451503-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,1,5,0 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 451503-21:
(8*4)+(7*5)+(6*1)+(5*5)+(4*0)+(3*3)+(2*2)+(1*1)=112
112 % 10 = 2
So 451503-21-2 is a valid CAS Registry Number.

451503-21-2Upstream product

451503-21-2Downstream Products

451503-21-2Relevant academic research and scientific papers

Asymmetric synthesis of diarylmethylamines by diastereoselective addition of organometallic reagents to chiral N-tert-butanesulfinimines: Switchover of diastereofacial selectivity

Plobeck, Niklas,Powell, David

, p. 303 - 310 (2007/10/03)

Diastereoselective addition of organometallic reagents to chiral N-tert-butanesulfinimines gave alkylated adducts in high yields and diastereoselectivities. Cleavage of the chiral auxiliary under mildly acidic conditions gave diarylmethylamines in high yi

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