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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)-

Benzo[b]thiophene-2-carboxylic acid, 3-chloro-, hydrazide

NNC(=O)c1sc2c(c1Cl)cccc2 Request for Quotation
Chemical Name: Benzo[b]thiophene-2-carboxylic acid, 3-chloro-, hydrazide
CAS Number: 62524-21-4
Product Number: AG00E9VF(AGN-PC-0JTOX6)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2OS
Molecular Weight: 226.6827

Identification/Properties

Computed Properties
Molecular Weight:
226.678g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
225.997g/mol
Monoisotopic Mass:
225.997g/mol
Topological Polar Surface Area:
83.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
239
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chlorobenzo[b]thiophene-2-carbohydrazide is a versatile chemical compound used in various chemical synthesis applications. This compound's unique structure and properties make it a valuable building block in organic synthesis and pharmaceutical research. In chemical synthesis, 3-Chlorobenzo[b]thiophene-2-carbohydrazide serves as a key intermediate in the production of a wide range of compounds, including heterocyclic derivatives and potential drug candidates. Its functional groups and reactivity make it suitable for forming diverse chemical bonds and enabling the synthesis of complex molecules.One of the notable applications of 3-Chlorobenzo[b]thiophene-2-carbohydrazide is in the development of novel pharmaceutical compounds. By incorporating this compound into the molecular structure of drug candidates, researchers can explore its pharmacological properties and potential therapeutic benefits. Additionally, its presence in the chemical structure can impart specific biological activities or enhance the efficacy of the resulting compounds.Furthermore, 3-Chlorobenzo[b]thiophene-2-carbohydrazide can be utilized in the synthesis of agrochemicals, dyes, and materials with tailored properties. Its versatility in chemical transformations and compatibility with various synthetic routes make it a valuable tool for designing and producing new functional molecules for different industrial applications.Overall, 3-Chlorobenzo[b]thiophene-2-carbohydrazide plays a crucial role in advancing chemical synthesis capabilities and expanding the scope of organic chemistry research. Its multifaceted applications and potential for generating diverse compounds make it a valuable reagent in the hands of chemists and researchers striving to innovate in the field of synthetic chemistry.