Cas 1044282-72-5,(R)-C-(3,5-dimethyl-phenyl)-C-(4-methoxycarbonyl-phenyl)-methyl-ammonium chloride

1044282-72-5

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Basic information

Product Name: (R)-C-(3,5-dimethyl-phenyl)-C-(4-methoxycarbonyl-phenyl)-methyl-ammonium chloride
Synonyms:
CAS NO:1044282-72-5
Molecular Formula:
Molecular Weight: 305.804
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)-C-(3,5-dimethyl-phenyl)-C-(4-methoxycarbonyl-phenyl)-methyl-ammonium chloride(CAS DataBase Reference)
NIST Chemistry Reference: (R)-C-(3,5-dimethyl-phenyl)-C-(4-methoxycarbonyl-phenyl)-methyl-ammonium chloride(1044282-72-5)
EPA Substance Registry System: (R)-C-(3,5-dimethyl-phenyl)-C-(4-methoxycarbonyl-phenyl)-methyl-ammonium chloride(1044282-72-5)

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: 1044282-72-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1044282-72-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,2,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1044282-72:
(9*1)+(8*0)+(7*4)+(6*4)+(5*2)+(4*8)+(3*2)+(2*7)+(1*2)=125
125 % 10 = 5
So 1044282-72-5 is a valid CAS Registry Number.

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1044282-72-5Relevant academic research and scientific papers

Conversion of 1,3-disubstituted arenes to chiral α,α-diaryl methylammonium chlorides using arene borylation

Boebel, Timothy A.,Hartwig, John F.

, p. 6824 - 6830 (2008)

A two-step conversion of 1,3-disubstituted arenes to chiral α,α-diaryl methylammonium chlorides is described. In this procedure, arenes are converted to aryl boronic esters by iridium-catalyzed borylation, and the aryl boronic esters are converted to enantioenriched amines by subsequent rhodium-catalyzed addition to chiral tert-butanesulfinimes.

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