1. Home
  2. Pyrazinecarboxylic acid, hydrazide

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrazinecarboxylic acid, hydrazide

NNC(=O)c1cnccn1 Request for Quotation
Chemical Name: Pyrazinecarboxylic acid, hydrazide
CAS Number: 768-05-8
Product Number: AG0035JO(AGN-PC-0JNV19)
Synonyms:
MDL No:
Molecular Formula: C5H6N4O
Molecular Weight: 138.1273

Identification/Properties

Properties
MP:
169°C
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
138.13g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
138.054g/mol
Monoisotopic Mass:
138.054g/mol
Topological Polar Surface Area:
80.9A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
127
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Pyrazinoic acid hydrazide is a versatile compound widely used in chemical synthesis for its unique properties and diverse applications. This compound serves as a valuable building block in the creation of various organic compounds, pharmaceuticals, and specialty chemicals. Its hydrazide functional group enables it to participate in a myriad of chemical reactions, such as acylation, alkylation, condensation, and more, making it a key component in the synthesis of complex molecules.In organic synthesis, pyrazinoic acid hydrazide is commonly employed as a nucleophilic reagent for the formation of C-N bonds, C-O bonds, and other important carbon-carbon bonds. Its reactivity and ability to undergo selective transformations make it an essential tool for chemists working on the synthesis of new compounds with specific properties or biological activities. Researchers utilize pyrazinoic acid hydrazide in the development of pharmaceuticals, agrochemicals, and materials science due to its structural diversity and reactivity profiles.Furthermore, in the field of medicinal chemistry, pyrazinoic acid hydrazide plays a crucial role as a valuable intermediate in the preparation of bioactive molecules and drug candidates. Its presence in drug discovery programs and process development underscores its importance as a key reagent in the pharmaceutical industry. Overall, the versatile nature and synthetic utility of pyrazinoic acid hydrazide make it an indispensable tool for chemists seeking to design and access novel compounds for a wide range of applications.