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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)-

6-fluoro-1,3-benzodioxol-5-amine

Fc1cc2OCOc2cc1N Request for Quotation
Chemical Name: 6-fluoro-1,3-benzodioxol-5-amine
CAS Number: 1366234-03-8
Product Number: AG00HUO8(AGN-PC-0H3MSV)
Synonyms:
MDL No: MFCD22069751
Molecular Formula: C7H6FNO2
Molecular Weight: 155.1264432

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Amino-6-fluoro-1,3-benzodioxole is a versatile compound widely utilized in chemical synthesis for its unique properties and applications. In organic chemistry, this compound serves as a crucial building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. The amino and fluoro functional groups present in 5-Amino-6-fluoro-1,3-benzodioxole provide opportunities for selective derivatization and enable the creation of diverse molecular structures. Its reactivity allows for the introduction of these functional groups into more complex molecules, making it a valuable tool in the hands of synthetic chemists. Additionally, the benzodioxole ring system contributes to the compound's stability and enhances its compatibility in different reaction conditions. Whether used as a nucleophilic or electrophilic reagent, 5-Amino-6-fluoro-1,3-benzodioxole plays a vital role in the synthesis of bioactive compounds and advanced materials, highlighting its significance in modern organic chemistry practices.