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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)-

tert-butyl N-[3-bromo-1-(2-fluorophenyl)propyl]carbamate

BrCCC(c1ccccc1F)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-[3-bromo-1-(2-fluorophenyl)propyl]carbamate
CAS Number: 924818-00-8
Product Number: AG00IH5P(AGN-PC-04Q6O0)
Synonyms:
MDL No: MFCD06410613
Molecular Formula: C14H19BrFNO2
Molecular Weight: 332.2085632

Identification/Properties

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 tert-Butyl (3-bromo-1-(2-fluorophenyl)propyl)carbamate is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the preparation of various organic molecules with specialized applications. It is commonly employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to introduce both the tert-butyl and carbamate functionalities into target molecules. Additionally, the presence of the bromo and fluoro substituents in the structure further enhances its utility in diverse synthetic pathways, enabling the introduction of additional functional groups or facilitating specific reaction mechanisms. The tert-Butyl (3-bromo-1-(2-fluorophenyl)propyl)carbamate demonstrates excellent stability under a wide range of reaction conditions, making it a valuable tool for chemists seeking to streamline complex synthesis routes and achieve high-yielding transformations.