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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-(chloromethyl)-3,5-difluoro-

ClCc1cc(F)cc(c1)F Request for Quotation
Chemical Name: Benzene, 1-(chloromethyl)-3,5-difluoro-
CAS Number: 220141-71-9
Product Number: AG003IMU(AGN-PC-0KK86Q)
Synonyms:
MDL No:
Molecular Formula: C7H5ClF2
Molecular Weight: 162.5644

Identification/Properties

Properties
BP:
164.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Stability:
Lachrymatory
Refractive Index:
1.4885
Computed Properties
Molecular Weight:
162.564g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
162.005g/mol
Monoisotopic Mass:
162.005g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.8
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#:
1760
Hazard Statements:
H314-H318
Precautionary Statements:
P260-P303+P361+P353-P305+P351+P338-P301+P330+P331-P405-P501
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzene, 1-(chloromethyl)-3,5-difluoro-, is a valuable compound widely used in chemical synthesis for its unique properties and diverse applications. This compound serves as a versatile building block in organic synthesis, offering a chloromethyl group and difluoro substituents that can be selectively modified and manipulated to create a variety of compounds.In chemical synthesis, Benzene, 1-(chloromethyl)-3,5-difluoro-, acts as a key intermediate for the preparation of complex molecules and pharmaceuticals. The chloromethyl group provides a reactive site for further functionalization reactions, allowing for the introduction of various functional groups to the benzene ring. Additionally, the presence of difluoro substituents contributes to the compound's electronic properties, influencing its reactivity and potential applications in medicinal chemistry and materials science.Overall, Benzene, 1-(chloromethyl)-3,5-difluoro-, plays a crucial role in the design and synthesis of innovative compounds with tailored properties, making it a valuable tool for researchers and chemists in the field of organic chemistry.