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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)-

Benzeneacetyl chloride, 4-chloro-

ClC(=O)Cc1ccc(cc1)Cl Request for Quotation
Chemical Name: Benzeneacetyl chloride, 4-chloro-
CAS Number: 25026-34-0
Product Number: AG0033ZU(AGN-PC-0JLYT7)
Synonyms:
MDL No:
Molecular Formula: C8H6Cl2O
Molecular Weight: 189.0386

Identification/Properties

Properties
BP:
254.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Liquid
Stability:
Moisture Sensitive
Refractive Index:
n20/D 1.5510(lit.)
Computed Properties
Molecular Weight:
189.035g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
187.98g/mol
Monoisotopic Mass:
187.98g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
139
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:
Danger
UN#:
3261
Hazard Statements:
H302-H312-H314-H332
Precautionary Statements:
P260-P261-P264-P270-P271-P280-P301+P312-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P312-P321-P322-P330-P363-P405-P501
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Chlorophenyl)acetyl chloride, also known as 4-Chlorobenzoyl chloride, is a versatile reagent widely used in chemical synthesis for various applications. This compound is frequently employed in organic chemistry as an acylating agent to introduce the acetyl group onto various nucleophiles. Its unique reactivity allows for the selective acylation of compounds containing nucleophilic functional groups, such as amines and alcohols.In organic synthesis, 2-(4-Chlorophenyl)acetyl chloride is commonly utilized for the preparation of amides, esters, and ketones through acylation reactions. It serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Furthermore, this compound can also be utilized in the preparation of various acetyl derivatives, which are important building blocks in the synthesis of complex organic molecules.Its ease of handling and compatibility with a wide range of solvents make 2-(4-Chlorophenyl)acetyl chloride a valuable tool in organic synthesis laboratories. Researchers and chemists rely on its reactivity and selectivity to achieve efficient and precise chemical transformations in the development of new compounds and materials.In conclusion,