Cas 1362019-72-4,(2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate

1362019-72-4

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Basic information

Product Name: (2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate
Synonyms: (2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate
CAS NO:1362019-72-4
Molecular Formula:
Molecular Weight: 299.345
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: (2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate(1362019-72-4)
EPA Substance Registry System: (2S,3S)-ethyl 2-(4-fluorophenyl)-1,2,3,4-tetrahydroquinoline-3-carboxylate(1362019-72-4)

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: 1362019-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1362019-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,0,1 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1362019-72:
(9*1)+(8*3)+(7*6)+(6*2)+(5*0)+(4*1)+(3*9)+(2*7)+(1*2)=134
134 % 10 = 4
So 1362019-72-4 is a valid CAS Registry Number.

1362019-72-4Upstream product

1362019-72-4Downstream Products

1362019-72-4Relevant academic research and scientific papers

Step-economical synthesis of tetrahydroquinolines by asymmetric relay catalytic Friedlaender condensation/transfer hydrogenation

Ren, Lei,Lei, Tao,Ye, Jia-Xi,Gong, Liu-Zhu

, p. 771 - 774 (2012)

Two steps in one reaction: The title relay reaction relies on a combination of an achiral Lewis acid and a chiral Bronsted acid (B-H in the scheme). This one-pot method provides access to tetrahydroquinoline derivatives with multiple continuous stereogeni

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