Cas 1437308-06-9,(2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate

1437308-06-9

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Basic information

Product Name: (2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate
Synonyms: (2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate
CAS NO:1437308-06-9
Molecular Formula:
Molecular Weight: 490.402
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: (2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate(1437308-06-9)
EPA Substance Registry System: (2R,4S)-dimethyl 2-methyl-6-(trifluoromethyl)-4-((4-(trifluoromethyl)phenyl)amino)-1,2,3,4-tetrahydroquinoline-2,4-dicarboxylate(1437308-06-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1437308-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1437308-06-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,7,3,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1437308-06:
(9*1)+(8*4)+(7*3)+(6*7)+(5*3)+(4*0)+(3*8)+(2*0)+(1*6)=149
149 % 10 = 9
So 1437308-06-9 is a valid CAS Registry Number.

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1437308-06-9Relevant academic research and scientific papers

A highly diastereo- and enantioselective synthesis of tetrahydroquinolines: Quaternary stereogenic center inversion and functionalization

Luo, Chaosheng,Huang, Yong

, p. 8193 - 8196 (2013)

Tetrahydroquinolines containing two quaternary stereogenic centers were synthesized with excellent ee and dr via a four-component cyclization reaction catalyzed by a chiral phosphoric acid. High chemoselectivity was achieved by differentiating anilines with similar reactivities to yield diverse hybrid products. The chirality of the quaternary C4 atom of the 4-aminotetrahydroquinoline products was found to undergo highly stereoselective inversion, enabling facile functionalization using a wide range of nucleophiles (C, O, N, and S).

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