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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)-

Benzoic acid,2,5-dimethoxy-, hydrazide

COc1ccc(c(c1)C(=O)NN)OC Request for Quotation
Chemical Name: Benzoic acid,2,5-dimethoxy-, hydrazide
CAS Number: 17894-25-6
Product Number: AG0026IY(AGN-PC-0QBG5X)
Synonyms:
MDL No:
Molecular Formula: C9H12N2O3
Molecular Weight: 196.2032

Identification/Properties

Properties
MP:
89-91°C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
196.206g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
196.085g/mol
Monoisotopic Mass:
196.085g/mol
Topological Polar Surface Area:
73.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
199
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,5-Dimethoxybenzohydrazide is a versatile chemical compound that finds wide application in the field of chemical synthesis. It serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique chemical properties, 2,5-Dimethoxybenzohydrazide is commonly used as a reagent in the synthesis of heterocyclic compounds and complex organic molecules.In organic synthesis, 2,5-Dimethoxybenzohydrazide plays a crucial role as a valuable precursor for the preparation of diverse functional groups and chemical structures. It serves as a key intermediate in the formation of hydrazones, which are important synthetic intermediates with a wide range of applications. Additionally, 2,5-Dimethoxybenzohydrazide can be utilized in the synthesis of various biologically active compounds, making it an essential compound in medicinal chemistry research.Overall, the versatile nature of 2,5-Dimethoxybenzohydrazide makes it a valuable tool in the hands of synthetic chemists for the efficient and precise construction of complex organic molecules with diverse applications.