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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)-

1-(chloromethyl)-2-(phenylmethyl)benzene

ClCc1ccccc1Cc1ccccc1 Request for Quotation
Chemical Name: 1-(chloromethyl)-2-(phenylmethyl)benzene
CAS Number: 7510-28-3
Product Number: AG003D2S(AGN-PC-0WA3XR)
Synonyms:
MDL No:
Molecular Formula: C14H13Cl
Molecular Weight: 216.7060

Identification/Properties

Properties
BP:
318.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
216.708g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
3
Exact Mass:
216.071g/mol
Monoisotopic Mass:
216.071g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
172
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzyl-2-(chloromethyl)benzene is a versatile compound commonly used in chemical synthesis due to its unique reactivity and functional group compatibility. This compound serves as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fine chemicals. In organic chemistry, 1-Benzyl-2-(chloromethyl)benzene is often employed as a building block for the introduction of a benzyl-protected benzene ring into complex molecular structures. Its chloromethyl group allows for further derivatization, such as nucleophilic substitution or cross-coupling reactions, enabling the synthesis of diverse chemical entities with specific properties and functionalities. Additionally, the benzyl group offers stability and can be selectively removed under mild conditions to reveal the active benzene functionality for subsequent chemical transformations. This compound's utility in chemical synthesis extends to the creation of novel materials, catalysts, and bioactive compounds, highlighting its significance in modern synthetic chemistry practices.