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t-Butyl (1-bromopropan-2-yl)carbamate

CAS 1391026-59-7Formula C8H16BrNO2MW 238.12PubChem 22274345

t-Butyl (1-bromopropan-2-yl)carbamate is a functionalized intermediate featuring a Boc-protected amine and a bromine atom. It serves as a versatile building block in organic synthesis, particularly for introducing protected amino-propyl or bromo-propyl groups into target molecules. This compound is for research use only.

Loading RDKit molecule structure...
InChIKey: OTOODTHBNJYOIV-UHFFFAOYSA-NC8H16BrNO2 | MW 238.12

Chemical Identity

Molecular Formula

C8H16BrNO2

Molecular Weight

238.12 g/mol

Exact Mass

237.03644

PubChem CID

22274345

IUPAC Name

tert-butyl N-(1-bromopropan-2-yl)carbamate

SMILES String

CC(CBr)NC(=O)OC(C)(C)C

Names & Synonyms

820-497-5tert-butyl (1-bromopropan-2-yl)carbamateC8H16BrNO2(S)-Tert-butyl 1-bromopropan-2-ylcarbamateN-Boc-1-bromo-2-propanamine
Show all synonyms
OTOODTHBNJYOIV-UHFFFAOYSA-Ntert-butyl(1-bromopropan-2-yl)carbamatetert-butyl N-(2-bromo-1-methyl-ethyl)carbamateF619176Carbamic acid, [(1S)-2-bromo-1-methylethyl]-, 1,1-dimethylethyl ester
External Identifiers
RefChem:890151MFCD24167884SCHEMBL1393407RFC02659AKOS026730029AS-35818SY238248DB-210189CS-0139502EN300-170177

Catalog Overview

t-Butyl (1-bromopropan-2-yl)carbamate, also known as tert-butyl N-(1-bromopropan-2-yl)carbamate, is an organic compound with the chemical formula C8H16BrNO2. It features a tert-butyl carbamate (Boc) protecting group on an amine and a bromine atom on an adjacent carbon, making it a versatile functionalized intermediate. This compound is typically employed in organic synthesis as a building block for the introduction of protected amino-propyl or bromo-propyl moieties into more complex molecular structures. Its reactivity stems from the bromine atom, which can undergo various nucleophilic substitution reactions, while the Boc group...

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Read more catalog context

t-Butyl (1-bromopropan-2-yl)carbamate, also known as tert-butyl N-(1-bromopropan-2-yl)carbamate, is an organic compound with the chemical formula C8H16BrNO2. It features a tert-butyl carbamate (Boc) protecting group on an amine and a bromine atom on an adjacent carbon, making it a versatile functionalized intermediate. This compound is typically employed in organic synthesis as a building block for the introduction of protected amino-propyl or bromo-propyl moieties into more complex molecular structures. Its reactivity stems from the bromine atom, which can undergo various nucleophilic substitution reactions, while the Boc group protects the amine functionality during these transformations. It is intended for research use only.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white solid

Physical State

solid

Melting Point

40.4 °C

Boiling Point

230.9 °C

Density

1.23 g/cm³

Water Solubility

7.59 × 10⁻³ mol/L

Flash Point

119.3 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or under a fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for detailed hazard information and handling procedures. This product is for research use only and not for human or animal therapeutic or diagnostic use.

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