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10128-92-4

3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10128-92-4 Structure

  • Basic information

    1. Product Name: 3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI)
    2. Synonyms: 3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI);3-Pyridinecarboxamide, 1,2-dihydro-2-oxo-
    3. CAS NO:10128-92-4
    4. Molecular Formula: C6H6N2O2
    5. Molecular Weight: 138.124
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 10128-92-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 528.7 °C at 760 mmHg
    3. Flash Point: 273.6 °C
    4. Appearance: /
    5. Density: 1.354 g/cm3
    6. Vapor Pressure: 2.89E-11mmHg at 25°C
    7. Refractive Index: 1.578
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI)(10128-92-4)
    12. EPA Substance Registry System: 3-Pyridinecarboxamide,1,2-dihydro-2-oxo-(9CI)(10128-92-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10128-92-4(Hazardous Substances Data)

10128-92-4 Usage

Uses

2-Hydroxynicotinamide has tuberculostatic activity.

Check Digit Verification of cas no

The CAS Registry Mumber 10128-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10128-92:
(7*1)+(6*0)+(5*1)+(4*2)+(3*8)+(2*9)+(1*2)=64
64 % 10 = 4
So 10128-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c7-5(9)4-2-1-3-8-6(4)10/h1-3H,(H2,7,9)(H,8,10)

10128-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-1H-pyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 2-oxo-1,2-dihydropyridine-3-carboxamide

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:10128-92-4 SDS

10128-92-4Relevant articles and documents

Direct Conversion of Haloarenes to Phenols under Mild, Transition-Metal-Free Conditions

Fier, Patrick S.,Maloney, Kevin M.

supporting information, p. 2244 - 2247 (2016/06/01)

A high-yielding and practical method for the synthesis of phenols from electron-deficient haloarenes and heteroarenes has been developed. The products are formed from acetohydroxamic acid as the hydroxide source via a novel SNAr reaction/Lossen rearrangement sequence. Notably, these reactions employ inexpensive and air-stable reagents, require no special handling, occur under mildly basic conditions, and form products in high yields in the presence of electrophilic and protic functionality. The utility of this methodology is demonstrated by the high-yielding hydroxylation of two base-sensitive complex substrates.

Synthesis and biological evaluation of pyridin-2-one nucleosides

Huntley,Cotterill,Maillard,Balzarini,Simons

, p. 731 - 733 (2007/10/03)

The synthesis of 1-(β -D-ribofuranosyl)pyridin-2-one-3-carboxylic acid and the 3-carboxamide as well as a short series of 3N-carboxamides, prepared by TPTU/HOBt coupling of primary amines with 1- (β-D-ribofuranosyl)pyridin-2-one-3-carboxylic acid, and the

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