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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)-

4-fluoro-1,3-benzodioxole

Fc1cccc2c1OCO2 Request for Quotation
Chemical Name: 4-fluoro-1,3-benzodioxole
CAS Number: 943830-74-8
Product Number: AG003LF1(AGN-PC-0NKWI8)
Synonyms:
MDL No:
Molecular Formula: C7H5FO2
Molecular Weight: 140.1118

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
140.113g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
140.027g/mol
Monoisotopic Mass:
140.027g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluorobenzo[d][1,3]dioxole, also known as $name$, is a versatile compound widely utilized in chemical synthesis processes. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. As a key intermediate, $name$ is valued for its ability to undergo diverse chemical reactions, enabling the synthesis of complex organic molecules with precision and efficiency. Its incorporation in synthetic routes allows for the modification of molecular structures, facilitating the development of novel compounds with enhanced biological or physical properties. In addition, 4-Fluorobenzo[d][1,3]dioxole plays a crucial role in the production of specialized reagents and catalysts, further expanding its utility in chemical transformations. This compound is a fundamental component in the toolbox of synthetic chemists, driving innovation and advancements in various fields of study.