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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)-

1H-Indole-3-acetic acid, hydrazide

NNC(=O)Cc1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 1H-Indole-3-acetic acid, hydrazide
CAS Number: 5448-47-5
Product Number: AG003EPD(AGN-PC-0JKFZ9)
Synonyms:
MDL No:
Molecular Formula: C10H11N3O
Molecular Weight: 189.2138

Identification/Properties

Properties
MP:
142-145 °C(lit.)
BP:
518 °C at 760 mmHg
Form:
Solid
Refractive Index:
1.4830 (estimate)
Computed Properties
Molecular Weight:
189.218g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
189.09g/mol
Monoisotopic Mass:
189.09g/mol
Topological Polar Surface Area:
70.9A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
219
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1H-Indol-3-yl)acetohydrazide is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the development of various organic molecules and pharmaceutical intermediates. With its indole and acetyl hydrazide functional groups, 2-(1H-Indol-3-yl)acetohydrazide offers a diverse range of synthetic pathways for the construction of complex structures. It can be employed in the synthesis of heterocyclic compounds, such as indole derivatives, as well as hydrazide-containing molecules. Additionally, 2-(1H-Indol-3-yl)acetohydrazide is a key starting material in the preparation of bioactive compounds and drug candidates, making it an essential tool for researchers in the pharmaceutical and chemical industries. Its strategic placement in organic synthesis strategies highlights its significance in achieving efficient and controlled chemical transformations, thereby enabling the exploration of new synthetic routes and the discovery of novel compounds with therapeutic potential.