Cas 280107-29-1,Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester

280107-29-1

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Basic information

Product Name: Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester
Synonyms: Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester
CAS NO:280107-29-1
Molecular Formula:
Molecular Weight: 521.458
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: Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester(280107-29-1)
EPA Substance Registry System: Trifluoro-methanesulfonic acid 2-{(R)-1-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethylamino]-ethyl}-phenyl ester(280107-29-1)

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: 280107-29-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 280107-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,0,1,0 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 280107-29:
(8*2)+(7*8)+(6*0)+(5*1)+(4*0)+(3*7)+(2*2)+(1*9)=111
111 % 10 = 1
So 280107-29-1 is a valid CAS Registry Number.

280107-29-1Upstream product

280107-29-1Downstream Products

280107-30-4 Trifluoro-methanesulfonic acid 2-((R)-1-{(2,2,2-trifluoro-acetyl)-[(R)-1-(2-trifluoromethanesulfonyloxy-phenyl)-ethyl]-amino}-ethyl)-phenyl ester

280107-29-1Relevant academic research and scientific papers

Diastereoselective synthesis of (5R,7R)- and (5R,7S)-5,7-dimethyl-6,7- dihydro-5H-dibenz[c,e]azepines

Saudan, Lionel A.,Bernardinelli, Gérald,Kündig, E. Peter

, p. 483 - 486 (2007/10/03)

Starting from (R)-1-(2-methoxyphenyl)ethylamine, the title compounds were synthesized. Key steps are a diastereoselective imine alkylation and a Pd-catalyzed biaryl coupling. The benzylic stereogenic centers of the (5R,7R)-azepine induce a strong bias for

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