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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, 3,4,5-trimethoxy-, hydrazide

NNC(=O)c1cc(OC)c(c(c1)OC)OC Request for Quotation
Chemical Name: Benzoic acid, 3,4,5-trimethoxy-, hydrazide
CAS Number: 3291-03-0
Product Number: AG003IEW(AGN-PC-0JLQ9P)
Synonyms:
MDL No:
Molecular Formula: C10H14N2O4
Molecular Weight: 226.2292

Identification/Properties

Properties
MP:
158-160°C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
226.232g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
226.095g/mol
Monoisotopic Mass:
226.095g/mol
Topological Polar Surface Area:
82.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
223
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


3,4,5-Trimethoxybenzohydrazide, also known as TMH, is a valuable compound widely utilized in chemical synthesis for various applications. In organic chemistry, TMH serves as a versatile building block due to its unique structure and reactivity. The primary role of 3,4,5-Trimethoxybenzohydrazide in chemical synthesis is as a precursor for the preparation of diverse heterocyclic compounds and pharmaceutical intermediates. Its hydrazide functional group allows for the formation of hydrazones and hydrazides, which are crucial intermediates in the synthesis of many organic molecules. Furthermore, TMH has been employed in the development of novel materials such as polymers and coordination complexes, showcasing its utility in the field of materials science. Additionally, 3,4,5-Trimethoxybenzohydrazide exhibits potential antimicrobial and anticancer properties, opening avenues for research in medicinal chemistry to explore its therapeutic applications. By virtue of its structural features and chemical reactivity, TMH continues to be a valuable compound in the toolbox of synthetic chemists for designing and synthesizing diverse functional molecules.