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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-(hexyloxy)-

CCCCCCOc1ccc(cc1)C(=O)Cl Request for Quotation
Chemical Name: Benzoyl chloride, 4-(hexyloxy)-
CAS Number: 39649-71-3
Product Number: AG003LU6(AGN-PC-0JPR9P)
Synonyms:
MDL No:
Molecular Formula: C13H17ClO2
Molecular Weight: 240.7259

Identification/Properties

Properties
BP:
213-214°C at 30 mmHg
Computed Properties
Molecular Weight:
240.727g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
7
Exact Mass:
240.092g/mol
Monoisotopic Mass:
240.092g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
198
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#:
3265
Hazard Statements:
H314-H318
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Hexyloxy)benzoyl chloride is a versatile chemical compound widely utilized in organic synthesis for various applications. As a benzoyl chloride derivative, it serves as an important acylating agent in the formation of esters, amides, and other functional groups. In chemical synthesis, this compound is commonly used as a reagent for the introduction of the hexyloxy group, which can impart specific properties to the target molecules. Additionally, it can participate in reactions such as Friedel-Crafts acylation and other transformations that require the selective acylation of aromatic compounds. The presence of the hexyloxy moiety in the benzoyl chloride structure allows for the synthesis of specialty chemicals, pharmaceutical intermediates, and advanced materials with tailored properties. Its strategic role in organic chemistry makes 4-(Hexyloxy)benzoyl chloride a valuable tool for the design and synthesis of diverse compounds with desired functionalities.