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62020-02-4

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62020-02-4 Usage

General Description

4-Nitropyridine-2-carboxamide is a chemical compound with the molecular formula C6H5N3O3. It is a yellow solid that is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 4-NITROPYRIDINE-2-CARBOXAMIDE is also known for its ability to form complexes with metal ions, making it useful in the field of coordination chemistry. It is a nitro derivative of pyridine-2-carboxamide and is often used as a building block in organic synthesis. Due to its potential toxic and harmful effects, proper safety precautions should be taken when handling and using 4-nitropyridine-2-carboxamide.

Check Digit Verification of cas no

The CAS Registry Mumber 62020-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,2 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62020-02:
(7*6)+(6*2)+(5*0)+(4*2)+(3*0)+(2*0)+(1*2)=64
64 % 10 = 4
So 62020-02-4 is a valid CAS Registry Number.
InChI:InChI=1S/C6H5N3O3/c7-6(10)5-3-4(9(11)12)1-2-8-5/h1-3H,(H2,7,10)

62020-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-nitropyridine-2-carboxamide

1.2 Other means of identification

Product number -
Other names 4-Nitro-picolinsaeureamid

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:62020-02-4 SDS

62020-02-4Upstream product

62020-02-4Downstream Products

62020-02-4Relevant articles and documents

Substrate-Specific Heterogeneous Catalysis of CeO2 by Entropic Effects via Multiple Interactions

Tamura, Masazumi,Sawabe, Kyoichi,Tomishige, Keiichi,Satsuma, Atsushi,Shimizu, Ken-Ichi

, p. 20 - 26 (2015/04/27)

Achieving complete substrate specificity through multiple interactions like an enzyme is one of the ultimate goals in catalytic studies. Herein, we demonstrate that multiple interactions between the CeO2 surface and substrates are the origin of substrate-specific hydration of nitriles in water by CeO2, which is exclusively applicable to the nitriles with a heteroatom (N or O) adjacent to the α-carbon of the CN group but is not applicable to the other nitriles. Kinetic studies reveal that CeO2 reduces the entropic barrier (TΔS?) for the reaction of the former reactive substrate, leading to 107-fold rate enhancement compared with the latter substrate. Density functional theory (DFT) calculations confirmed multiple interaction of the reactive substrate with CeO2, as well as preferable approximation and alignment of the nitrile group of the substrate to the active OH group on CeO2 surface. This can lead to the reduction of the entropic barrier. This is the first example of an entropy-driven substrate-specific catalysis of a nonporous metal oxide surface, which will provide a new design strategy for enzyme-inspired synthetic catalysts.

BENZAMIDE FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS

-

Page/Page column 76, (2010/09/17)

The present invention provides novel benzamide derivatives of Formula (I): or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein the variables A, W, Y, Z, R8, and R9 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

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