Cas 1133378-64-9,(2S,3S)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde

1133378-64-9

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Basic information

Product Name: (2S,3S)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde
Synonyms: (2S,3S)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde
CAS NO:1133378-64-9
Molecular Formula:
Molecular Weight: 343.425
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)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde(1133378-64-9)
EPA Substance Registry System: (2S,3S)-1-(4-methoxyphenyl)-2-(naphthalen-2-yl)-1,2,3,4-tetrahydropyridine-3-carbaldehyde(1133378-64-9)

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: 1133378-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133378-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,3,7 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1133378-64:
(9*1)+(8*1)+(7*3)+(6*3)+(5*3)+(4*7)+(3*8)+(2*6)+(1*4)=139
139 % 10 = 9
So 1133378-64-9 is a valid CAS Registry Number.

1133378-64-9Upstream product

1133378-64-9Downstream Products

1133378-64-9Relevant academic research and scientific papers

Proline-mediated enantioselective construction of tetrahydropyridines via a cascade Mannich-type/intramolecular cyclization reaction

Han, Rong-Gang,Wang, Yao,Li, Yu-Ye,Xu, Peng-Fei

supporting information; experimental part, p. 1474 - 1478 (2009/07/18)

A highly diastereo- and enantioselective synthesis of 2,3-disubstituted tetrahydropyridines was accomplished via a proline-mediated cascade Mannich-type/intramolecular cyclization reaction from preformed N-PMP (p-methoxyphenyl) aldimines and inexpensive aqueous tetrahydro-2H-pyran-2,6- diol.

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