Cas 1245527-98-3,methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate

1245527-98-3

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Basic information

Product Name: methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate
Synonyms: methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate
CAS NO:1245527-98-3
Molecular Formula:
Molecular Weight: 343.379
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-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate(1245527-98-3)
EPA Substance Registry System: methyl-1-(3,4-dimethoxybenzyl)-4-oxo-6-(prop-1-ynyl)-1,4,5,6-tetrahydropyridine-2-carboxylate(1245527-98-3)

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: 1245527-98-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1245527-98-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,5,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1245527-98:
(9*1)+(8*2)+(7*4)+(6*5)+(5*5)+(4*2)+(3*7)+(2*9)+(1*8)=163
163 % 10 = 3
So 1245527-98-3 is a valid CAS Registry Number.

1245527-98-3Upstream product

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1245527-98-3Relevant academic research and scientific papers

Synthesis of cylindricine C and a formal synthesis of cylindricine A

Donohoe, Timothy J.,Brian, Ptoton M.,Hargaden, Gráinne C.,O'Riordan, Timothy J.C.

experimental part, p. 6411 - 6420 (2010/10/18)

This paper reports the synthesis of the alkaloid natural product (±)-cylindricine C, in addition to a formal synthesis of (±)-cylindricine A. The key step in our sequence is the (ipso) regioselective addition of an alkyl Grignard reagent to a C-2 substitu

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