Cas 1261268-44-3,methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate

1261268-44-3

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Basic information

Product Name: methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate
Synonyms: methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate
CAS NO:1261268-44-3
Molecular Formula:
Molecular Weight: 417.913
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: methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate(1261268-44-3)
EPA Substance Registry System: methyl (+/-)-6-(4-chlorophenyl)-1,6-dihydro-4-methyl-1-tosylpyridine-3-carboxylate(1261268-44-3)

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: 1261268-44-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1261268-44-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,6 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1261268-44:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*6)+(3*8)+(2*4)+(1*4)=143
143 % 10 = 3
So 1261268-44-3 is a valid CAS Registry Number.

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1261268-44-3Relevant academic research and scientific papers

Synthesis of substituted 1,2-dihydropyridines from propargyl vinyl ethers and allenic vinyl ethers by gold-catalyzed claisen rearrangement and 6π-aza-electrocyclization

Wei, Hao,Wang, Yao,Yue, Bin,Xu, Peng-Fei

experimental part, p. 2450 - 2454 (2010/12/25)

An efficient synthetic method was developed for the construction of substituted 1,2-dihydropyridines by gold-catalyzed tandem reactions. The key intermediates 2,4-dienals were generated from propargyl vinyl ethers or allenic vinyl ethers with gold catalys

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