Atomfair tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate C13H18BrNO2

Description tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate (CAS No. 847728-89-6) is a high-purity organic compound with the molecular formula C13H18BrNO2. This carbamate derivative features a tert-butyloxycarbonyl (Boc) protecting group and a 4-bromophenyl substituent, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The compound is characterized by its white to off-white crystalline appearance and is supplied with ??95% purity (HPLC). It is stable under inert conditions but sensitive to strong acids and bases. Ideal for researchers in medicinal chemistry, this reagent is packaged under argon in amber glass vials to ensure long-term stability. Storage at 2-8??C is recommended.

Description

tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate (CAS No. 847728-89-6) is a high-purity organic compound with the molecular formula C₁₃H₁₈BrNO₂. This carbamate derivative features a tert-butyloxycarbonyl (Boc) protecting group and a 4-bromophenyl substituent, making it a valuable intermediate in pharmaceutical and agrochemical synthesis. The compound is characterized by its white to off-white crystalline appearance and is supplied with ??95% purity (HPLC). It is stable under inert conditions but sensitive to strong acids and bases. Ideal for researchers in medicinal chemistry, this reagent is packaged under argon in amber glass vials to ensure long-term stability. Storage at 2-8??C is recommended.

CAS No: 847728-89-6
Molecular Formula: C13H18BrNO2
Molecular Weight: 300.19
Exact Mass: 299.05209
Monoisotopic Mass: 299.05209
IUPAC Name: tert-butyl N-[1-(4-bromophenyl)ethyl]carbamate
SMILES: CC(C1=CC=C(C=C1)Br)NC(=O)OC(C)(C)C
Synonyms: Tert-butyl N-[1-(4-bromophenyl)ethyl]carbamate, tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate, 809-643-9, 850363-42-7, tert-Butyl (1-(4-bromophenyl)ethyl)carbamate

Application

tert-butyl N-(1-(4-bromophenyl)ethyl)carbamate is widely used as a key building block in the synthesis of active pharmaceutical ingredients (APIs) and fine chemicals. Its Boc-protected amine group allows for selective deprotection in multi-step reactions, particularly in peptidomimetics and small-molecule drug development. The 4-bromophenyl moiety enables further functionalization via cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig amination. Researchers also employ it in the preparation of chiral auxiliaries and ligands for asymmetric catalysis.

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