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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)-

Benzoyl chloride, 4-(dimethylamino)-, hydrochloride

CN(c1ccc(cc1)C(=O)Cl)C.Cl Request for Quotation
Chemical Name: Benzoyl chloride, 4-(dimethylamino)-, hydrochloride
CAS Number: 149898-87-3
Product Number: AG001M3Q(AGN-PC-03JOS3)
Synonyms:
MDL No:
Molecular Formula: C9H11Cl2NO
Molecular Weight: 220.0957

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
220.093g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
219.022g/mol
Monoisotopic Mass:
219.022g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
162
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 4-(Dimethylamino)benzoyl chloride hydrochloride is commonly used as a reagent for acylation reactions. This compound serves as an acylating agent, allowing for the introduction of the 4-(Dimethylamino)benzoyl group onto various nucleophilic molecules. The hydrochloride salt form of this compound provides enhanced solubility in aqueous and polar organic solvents, making it a versatile choice for a wide range of synthetic procedures. Additionally, the presence of the dimethylamino group serves as a useful handle for further derivatization or manipulation of the molecule, enabling the synthesis of diverse chemical compounds with tailored properties.