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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)-

Benzene, (1-chloropropyl)-

CCC(c1ccccc1)Cl Request for Quotation
Chemical Name: Benzene, (1-chloropropyl)-
CAS Number: 934-11-2
Product Number: AG006FY5(AGN-PC-0JSBL6)
Synonyms:
MDL No:
Molecular Formula: C9H11Cl
Molecular Weight: 154.6366

Identification/Properties

Computed Properties
Molecular Weight:
154.637g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
154.055g/mol
Monoisotopic Mass:
154.055g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
84.7
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
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


The (1-Chloropropyl)benzene is a versatile chemical compound commonly used in chemical synthesis processes. Its primary application lies in acting as a key intermediate in the production of various valuable compounds. This compound is particularly valued for its ability to undergo nucleophilic substitution reactions, where the chlorine atom can be easily replaced by a different functional group. This property makes (1-Chloropropyl)benzene a crucial building block in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and specialty chemicals. Additionally, its structure enables it to participate in various organic transformations, allowing for the creation of diverse chemical structures with specific properties and functionalities. In the realm of chemical synthesis, (1-Chloropropyl)benzene serves as a fundamental tool for chemists to design and construct intricate molecules with precision and efficiency.