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Tert-butyl (2-bromopropyl)carbamate

CAS 121102-88-3Formula C8H16BrNO2MW 238.12PubChem 14458310

Tert-butyl (2-bromopropyl)carbamate is a bromo-substituted carbamate derivative, commonly employed as a versatile building block in organic synthesis, particularly for introducing protected amine functionalities with a bromine leaving group.

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

Chemical Identity

Molecular Formula

C8H16BrNO2

Molecular Weight

238.12 g/mol

Exact Mass

237.03644

PubChem CID

14458310

IUPAC Name

tert-butyl N-(2-bromopropyl)carbamate

SMILES String

CC(Br)CNC(=O)OC(C)(C)C

Names & Synonyms

822-411-1N-Boc-2-bromo-1-propanamineCarbamic acid, (2-bromopropyl)-, 1,1-dimethylethyl esterKHFDEFLMWSUKAS-UHFFFAOYSA-Ntert-butyl(2-bromopropyl)carbamate
Show all synonyms
F387496
External Identifiers
RefChem:891581MFCD24167156SCHEMBL3526275WEA10288AKOS025243972AS-32501DA-47180SY028850CS-0442286EN300-1272499

Catalog Overview

Tert-butyl (2-bromopropyl)carbamate, with CAS 121102-88-3 and molecular formula C8H16BrNO2, is a key functionalized intermediate in synthetic chemistry. It features a tert-butyl carbamate (Boc) protecting group on an amine, alongside a bromine atom on the propyl chain. This bifunctional nature makes it highly valuable for various synthetic transformations, including nucleophilic substitution reactions to introduce new functionalities, or as a precursor in the synthesis of more complex molecules. Its Boc group provides amine protection, which can be selectively removed under acidic conditions, allowing for controlled reactivity in...

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

Tert-butyl (2-bromopropyl)carbamate, with CAS 121102-88-3 and molecular formula C8H16BrNO2, is a key functionalized intermediate in synthetic chemistry. It features a tert-butyl carbamate (Boc) protecting group on an amine, alongside a bromine atom on the propyl chain. This bifunctional nature makes it highly valuable for various synthetic transformations, including nucleophilic substitution reactions to introduce new functionalities, or as a precursor in the synthesis of more complex molecules. Its Boc group provides amine protection, which can be selectively removed under acidic conditions, allowing for controlled reactivity in multi-step syntheses. This compound 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

40.9 °C

Boiling Point

230.9 °C

Density

1.23 g/cm³

Water Solubility

0.0221 mol/L

Flash Point

133.8 °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 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. Always consult the Safety Data Sheet (SDS) for comprehensive safety information before use.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Similar products (text references)

2679839-22-4CAS 2679839-22-4

Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 29241990GHS Pictograms: GHS06, GHS07Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.

Catalog navigation

Other public CAS pages in this catalog. These links support navigation across additional intermediates and do not imply equivalence, availability, or shared use.