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2-METHYLCARBAMOYLISONICOTINIC ACID ETHYL ESTER is a chemical compound with the molecular formula C11H14N2O4. It is an ester derived from 2-methylcarbamoylisonicotinic acid and ethyl alcohol, and is a derivative of nicotinic acid, a type of B vitamin that plays a role in energy production and metabolism. The ethyl ester form of 2-methylcarbamoylisonicotinic acid is often used in research and pharmaceutical applications, particularly in the development of new drugs and treatments for various medical conditions. Its properties and potential uses make it a subject of interest in the fields of chemistry and pharmacology.

332013-42-0

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  • 4-Pyridinecarboxylicacid, 2-[(methylamino)carbonyl]-, ethyl ester

    Cas No: 332013-42-0

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332013-42-0 Usage

Uses

Used in Pharmaceutical Applications:
2-METHYLCARBAMOYLISONICOTINIC ACID ETHYL ESTER is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and treatments for a range of medical conditions.
Used in Research:
2-METHYLCARBAMOYLISONICOTINIC ACID ETHYL ESTER is used as a research compound in the fields of chemistry and pharmacology. Its unique properties and potential applications make it a valuable tool for studying the mechanisms of action and potential therapeutic uses of related compounds.
Used in Drug Development:
2-METHYLCARBAMOYLISONICOTINIC ACID ETHYL ESTER is used in the development of new drugs and treatments for various medical conditions. Its unique structure and properties make it a promising candidate for the development of novel therapeutic agents.
Used in Chemical Synthesis:
2-METHYLCARBAMOYLISONICOTINIC ACID ETHYL ESTER is used as a starting material or intermediate in the synthesis of other chemical compounds. Its unique structure and properties make it a valuable component in the production of a variety of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 332013-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,0,1 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 332013-42:
(8*3)+(7*3)+(6*2)+(5*0)+(4*1)+(3*3)+(2*4)+(1*2)=80
80 % 10 = 0
So 332013-42-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O3/c1-3-15-10(14)7-4-5-12-8(6-7)9(13)11-2/h4-6H,3H2,1-2H3,(H,11,13)

332013-42-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(methylcarbamoyl)pyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 2-[(METHYLAMINO)CARBONYL]-PYRIDINE-4-CARBOXYLIC ACID ETHYL ESTER

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:332013-42-0 SDS

332013-42-0Relevant articles and documents

Design, synthesis and biological evaluation of indole derivatives as novel inhibitors targeting B-Raf kinase

Wu, Zeng,Yan, Ming,Hu, Shi-He,Yu, Zhi-Cheng,Zhu, Yong,Cheng, Ya-Dong,Liu, Hai-Chun,Zhang, Yan-Min,Yao, Si-Hui,Tang, Wei-Fang,Lu, Tao

, p. 351 - 354 (2014/02/14)

A series of novel indole derivatives were designed and synthesized and their inhibitory activity against B-Raf and HepG2 cell were also described. Among them, compounds 7a and 7b exhibited excellent potency, which showed the potential for further research

SUBSTITUTED PYRIDINES AND PYRIDAZINES WITH ANGIOGENESIS INHIBITING ACTIVITY

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Page/Page column 41, (2009/03/07)

Substituted pyridines and pyridazines having angiogenesis inhibiting activity and generalized structural formula (I) wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R and R may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermeability processes using these materials are also disclosed.

COMPOUNDS FOR TREATING PULMONARY HYPERTENSION

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Page/Page column 62; 63, (2008/06/13)

The present invention relates to pharmaceutical compositions and combinations for treating, preventing or managing pulmonary hypertension comprising small molecule heterocyclic pharmaceuticals, and more particularly, substituted pyridines and pyridazines optionally combined with at least one additional therapeutic agent.

Substituted pyridines and pyridazines with angiogenesis inhibiting activity

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Page column 55-56, (2010/02/05)

Substituted pyridazines having angiogenesis inhibiting activity and the generalized structural formula wherein the ring containing A, B, D, E, and L is phenyl or a nitrogen-containing heterocycle; groups X and Y may be any of a variety of defined linking units; R1and R2may be defined independent substituents or together may be a ring-defining bridge; ring J may be an aryl, pyridyl, or cycloalkyl group; and G groups may be any of a variety of defined substituents. Pharmaceutical compositions containing these materials, and methods of treating a mammal having a condition characterized by abnormal angiogenesis or hyperpermiability processes using these materials are also disclosed.

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