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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)-

Benzamide, 4-chloro-N-(2-hydroxyethyl)-

OCCNC(=O)c1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzamide, 4-chloro-N-(2-hydroxyethyl)-
CAS Number: 7400-54-6
Product Number: AG005AEY(AGN-PC-0JOB5E)
Synonyms:
MDL No:
Molecular Formula: C9H10ClNO2
Molecular Weight: 199.6342

Identification/Properties

Computed Properties
Molecular Weight:
199.634g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
199.04g/mol
Monoisotopic Mass:
199.04g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
167
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-N-(2-hydroxyethyl)benzamide is a versatile compound commonly used in chemical synthesis for its valuable applications. In the realm of organic chemistry, this compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity make it an essential intermediate in the creation of complex molecular structures.One of the prominent applications of 4-Chloro-N-(2-hydroxyethyl)benzamide is in the synthesis of bioactive molecules with therapeutic potential. By incorporating this compound into the chemical structure of pharmaceuticals, researchers can modulate the biological activity and pharmacokinetic properties of the final products. This enables the development of novel drugs with improved efficacy and reduced side effects.Furthermore, 4-Chloro-N-(2-hydroxyethyl)benzamide plays a crucial role in the synthesis of specialty chemicals used in various industries. Its ability to undergo specific chemical reactions, such as nucleophilic substitution and coupling reactions, allows for the efficient production of high-value intermediates and final products. This compound facilitates the creation of advanced materials, dyes, and polymers that find applications in diverse sectors.Overall, the versatility and reactivity of 4-Chloro-N-(2-hydroxyethyl)benzamide make it a valuable tool in chemical synthesis, driving innovation and progress in the development of new compounds with diverse industrial and pharmaceutical applications.