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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)-

ethyl 3-hydrazinylbenzoate;hydrochloride

CCOC(=O)c1cccc(c1)NN.Cl Request for Quotation
Chemical Name: ethyl 3-hydrazinylbenzoate;hydrochloride
CAS Number: 940875-99-0
Product Number: AG00H32A(AGN-PC-079GVP)
Synonyms:
MDL No:
Molecular Formula: C9H13ClN2O2
Molecular Weight: 216.6647

Identification/Properties

Computed Properties
Molecular Weight:
216.665g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
216.067g/mol
Monoisotopic Mass:
216.067g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
173
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:
2
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

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Chemical Structure


Ethyl 3-hydrazinylbenzoate hydrochloride is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a crucial building block in the production of various organic compounds due to its unique structural properties. In the field of chemistry, it is commonly utilized as a reagent for the synthesis of heterocyclic compounds and pharmaceutical intermediates. Its hydrazine functionality enables it to participate in a range of important reactions, such as acylation, alkylation, and condensation reactions, leading to the formation of complex organic molecules. Additionally, the hydrochloride salt form of this compound enhances its stability and solubility in different reaction media, making it a valuable tool for chemists in designing and developing novel molecular structures in the laboratory.