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METHYL 2-METHYL-4-(3-NITROPHENYL)-6-OXO-1,4,5,6-TETRAHYDRO-3-PYRIDINECARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130734-38-2

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130734-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130734-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130734-38:
(8*1)+(7*3)+(6*0)+(5*7)+(4*3)+(3*4)+(2*3)+(1*8)=102
102 % 10 = 2
So 130734-38-2 is a valid CAS Registry Number.

130734-38-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 6-methyl-4-(3-nitrophenyl)-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 4-(3-nitrophenyl)-5-methoxycarbonyl-6-methyl-3,4-dihydropyridin-2(1H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:130734-38-2 SDS

130734-38-2Relevant academic research and scientific papers

Synthesis of 5-carboxy-6-methyl-3,4-dihydro-2(1H)-pyridone derivatives and their electrochemical oxidation to 2-pyridones

Smits, Rufus,Turovska, Baiba,Belyakov, Sergey,Plotniece, Aiva,Duburs, Gunars

, p. 84 - 87 (2016/04/04)

A series of variously substituted 5-carboxy-6-methyl-3,4-dihydro-2(1H)-pyridone derivatives were synthesized and their oxidation potentials determined by cyclic voltammetry. The resulting 2-pyridone structure and a tricyclic heterocycle which was formed d

Mesostructured SBA-15-Pr-SO3H: An efficient solid acid catalyst for one-pot and solvent-free synthesis of 3,4-dihydro-2-pyridone derivatives

Ziarani, Ghodsi Mohammadi,Mousavi, Somayeh,Lashgari, Negar,Badiei, Alireza

, p. 1359 - 1364 (2014/04/03)

3,4-Dihydro-2-pyridone derivatives have been prepared efficiently via a one-pot four-component reaction of benzaldehyde derivatives, Meldrum's acid, methyl acetoacetate and ammonium acetate in the presence of sulphonic acid-functionalized ordered nanoporo

Solvent-free synthesis of 4-aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones under microwave irradiation

Rodríguez, Hortensia,Suarez, Margarita,Pérez, Rolando,Petit, Alain,Loupy, André

, p. 3709 - 3712 (2007/10/03)

4-Aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones have been prepared in one-pot condensation from Meldrum's acid, methyl acetoacetate and the appropriate benzaldehyde in the presence of ammonium acetate using microwave irradiation without

Solid-phase synthesis of 4-aryl substituted 5-carboxy-6-methyl-3,4-dihydropyridones

Rodríguez, Hortensia,Reyes, Osvaldo,Suarez, Margarita,Garay, Hilda E.,Pérez, Rolando,Cruz, Luis Javier,Verdecia, Yamila,Martín, Nazario,Seoane, Carlos

, p. 439 - 441 (2007/10/03)

Substituted 3,4-dihydro-2-pyridones have been efficiently prepared by solid-phase synthesis using Wang resin from the immobilised β-ketoester and further Hantzsch-type heterocyclisation.

Novel hexahydrofuro[3,4-b]-2(1H)-pyridones from 4-aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones

Morales, Alhmed,Ochoa, Estael,Suarez, Margarita,Verdecia, Yamila,Gonzalez, Leandro,Martin, Nazario,Quinteiro, Margarita,Seoane, Carlos,Soto, Jose L.

, p. 103 - 107 (2007/10/03)

The title compounds 6 have been prepared in a one-step procedure from the corresponding 4-aryl substituted 5-alkoxycarbonyl-6-methyl-3,4-dihydropyridones 4 in good yields. Quantum chemical calculations reveal a non-planar molecule with a distorted dihydropyridone ring and two favoured conformations. The 13C nmr data and theoretical calculations support a strong push-pull effect on the olefinic moiety.

Synthesis of methyl 4-aryl-6-methyl-4,7-dihydro-1H-pyrazolo-[3,4-b]pyridine-5-carboxylates from methyl 4-aryl-6-methyl-2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylates

Verdecia, Yamila,Suarez, Margarita,Morales, Alhmed,Rodriguez, Elena,Ochoa, Estael,Gonzalez, Leandro,Martin, Nazario,Quinteiro, Margarita,Seoane, Carlos,Soto, Jose L.

, p. 947 - 951 (2007/10/03)

Novel methyl 4,7-dihydro-1H-pyrazolo[3,4-b]pyridine-5-carboxylates 3a-e have been prepared in a two step procedure from the readily available 2-oxo-1,2,3,4-tetrahydropyridine-5-carboxylates 1a-e by treatment with the Vilsmeier-Haack reagent. Further treat

Oxygen-bridged Tetrahydropyridines, Hexahydropyridines, and Dihydropyridones via a Hantzsch-like Synthesis with 4-(2-Hydroxyphenyl)but-3-en-2-one

Svetlik, Jan,Goljer, Igor,Turecek, Frantisek

, p. 1315 - 1318 (2007/10/02)

Substituted oxygen-bridged tetrahydro-2-pyridones and tetrahydropyridines (4) and (7) were synthesized by condensation of 4-(2-hydroxyphenyl)but-3-en-2-one (1) with Meldrum's acid (2) and 3-aminocrotononitrile, respectively, in the presence of ammonium ac

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