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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)-

Hydrazinecarboxamide, 1-methyl-

NC(=O)N(N)C Request for Quotation
Chemical Name: Hydrazinecarboxamide, 1-methyl-
CAS Number: 22718-48-5
Product Number: AG00I4GZ(AGN-PC-0JNT70)
Synonyms:
MDL No:
Molecular Formula: C2H7N3O
Molecular Weight: 89.0965

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
89.098g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
89.059g/mol
Monoisotopic Mass:
89.059g/mol
Topological Polar Surface Area:
72.4A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
61.8
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Methylhydrazinecarboxamide is a versatile compound that finds broad application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals and agrochemicals due to its ability to undergo diverse chemical transformations. In organic synthesis, 1-Methylhydrazinecarboxamide can participate in key reactions such as acylation, alkylation, and condensation reactions to form a wide range of functionalized compounds. Its reactivity with various electrophiles allows for the formation of complex structures, making it a valuable tool for the synthesis of biologically active molecules.Furthermore, 1-Methylhydrazinecarboxamide can be utilized as a precursor for the preparation of hydrazine derivatives, which are important intermediates in the synthesis of heterocyclic compounds and functional materials. Its unique combination of functional groups makes it a crucial starting material for the development of novel chemical entities with potential applications in the fields of medicine, agriculture, and materials science.