1. Home
  2. Acetic acid, methoxy-, 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)-

Acetic acid, methoxy-, hydrazide

COCC(=O)NN Request for Quotation
Chemical Name: Acetic acid, methoxy-, hydrazide
CAS Number: 20605-41-8
Product Number: AG002AIF(AGN-PC-0KKNAF)
Synonyms:
MDL No:
Molecular Formula: C3H8N2O2
Molecular Weight: 104.1078

Identification/Properties

Computed Properties
Molecular Weight:
104.109g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
104.059g/mol
Monoisotopic Mass:
104.059g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
64
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+H312+H332-H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Methoxyacetohydrazide is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group compatibility. This compound is predominantly employed as a key building block in the synthesis of various organic molecules and pharmaceutical compounds. Its inherent properties make it a valuable tool in the development of new drugs, agrochemicals, and materials.In chemical synthesis, 2-Methoxyacetohydrazide serves as a precursor in the preparation of hydrazones, which are important intermediates in many organic reactions. Additionally, it can be used for the synthesis of heterocyclic compounds and bioactive molecules due to its ability to participate in a wide range of transformations, such as acylation and condensation reactions.Moreover, the presence of the hydrazide functional group in 2-Methoxyacetohydrazide allows for the introduction of diverse functionalities through subsequent derivatization reactions. This enables chemists to modulate the properties of the final products and tailor them for specific applications, enhancing the versatility and utility of this compound in various synthetic pathways.Overall, the application of 2-Methoxyacetohydrazide in chemical synthesis underscores its significance as a valuable building block that enables the efficient and strategic construction of complex organic molecules with diverse functionalities and applications.