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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)-

Acetamide, N-(4-chlorophenyl)-2-cyano-

N#CCC(=O)Nc1ccc(cc1)Cl Request for Quotation
Chemical Name: Acetamide, N-(4-chlorophenyl)-2-cyano-
CAS Number: 17722-17-7
Product Number: AG00257J(AGN-PC-0JLWOK)
Synonyms:
MDL No:
Molecular Formula: C9H7ClN2O
Molecular Weight: 194.6177

Identification/Properties

Properties
MP:
207-209℃(lit.)
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
194.618g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
194.025g/mol
Monoisotopic Mass:
194.025g/mol
Topological Polar Surface Area:
52.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
225
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-H312-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(4-Chlorophenyl)-2-cyanoacetamide, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key intermediate. This compound plays a crucial role in the preparation of various organic molecules through its ability to undergo diverse reactions and transformations.One primary application of N-(4-Chlorophenyl)-2-cyanoacetamide is in the synthesis of pharmaceutical compounds. Its unique chemical structure enables it to serve as a building block for the construction of biologically active molecules, including pharmaceutical drugs and medicinal chemicals. By reacting with different reagents and functional groups, this compound can be modified to introduce specific functionalities or stereochemistries necessary for drug development.Additionally, N-(4-Chlorophenyl)-2-cyanoacetamide is utilized in the production of agrochemicals and specialty chemicals. Its incorporation into synthetic routes allows for the efficient construction of complex organic molecules with agricultural or industrial applications. Through strategic chemical transformations, this compound can be tailored to exhibit desired properties such as pesticidal activity or material compatibility.Furthermore, N-(4-Chlorophenyl)-2-cyanoacetamide finds use in academic research and chemical synthesis laboratories for the exploration of new reaction pathways and the development of novel compounds. Its flexibility in undergoing various chemical transformations makes it a valuable tool for organic chemists seeking to access diverse molecular structures and study their properties.In conclusion, N-(4-Chlorophenyl)-2-cyanoacetamide is a versatile compound with broad applications in chemical synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its role as an intermediate facilitates the efficient construction of complex organic molecules, making it an indispensable component in the synthesis of diverse compounds.