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Tert-butyl (R)-(4-chlorobutan-2-YL)carbamate

CAS 2170323-80-3Formula C9H18ClNO2MW 207.7PubChem 143051612

Tert-butyl (R)-(4-chlorobutan-2-YL)carbamate is a chiral functionalized intermediate with the chemical formula C9H18ClNO2. It is primarily used in research and development as a building block for synthesizing more complex organic molecules, particularly where stereospecificity is required.

Loading RDKit molecule structure...
InChIKey: DLIYJYQTVMUHFQ-SSDOTTSWSA-NC9H18ClNO2 | MW 207.7

Chemical Identity

Molecular Formula

C9H18ClNO2

Molecular Weight

207.7 g/mol

Exact Mass

207.102607

PubChem CID

143051612

IUPAC Name

tert-butyl N-[(2R)-4-chlorobutan-2-yl]carbamate

SMILES String

C[C@H](CCCl)NC(=O)OC(C)(C)C

External Identifiers
AT31957EN300-28272675

Catalog Overview

Tert-butyl (R)-(4-chlorobutan-2-YL)carbamate, identified by CAS 2170323-80-3, is a precisely structured organic compound featuring a tert-butyl carbamate protecting group and a chiral center at the second carbon of the butane chain, along with a terminal chlorine atom. With a molecular weight of 207. 70 g/mol, this compound serves as a versatile chiral building block in synthetic organic chemistry. Its specific (R)-configuration makes it valuable for stereoselective synthesis, particularly in the preparation of pharmaceutical intermediates and other fine chemicals where chirality is critical.

Use Context

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

Tert-butyl (R)-(4-chlorobutan-2-YL)carbamate, identified by CAS 2170323-80-3, is a precisely structured organic compound featuring a tert-butyl carbamate protecting group and a chiral center at the second carbon of the butane chain, along with a terminal chlorine atom. With a molecular weight of 207.70 g/mol, this compound serves as a versatile chiral building block in synthetic organic chemistry. Its specific (R)-configuration makes it valuable for stereoselective synthesis, particularly in the preparation of pharmaceutical intermediates and other fine chemicals where chirality is critical. Researchers utilize this functionalized intermediate for various coupling reactions, nucleophilic substitutions, and other transformations to construct desired molecular architectures for research purposes.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

Colorless liquid

Physical State

Liquid

Melting Point

5.0 °C

Boiling Point

220.0 °C

Density

1.05 g/cm³

Water Solubility

Sparingly soluble

Flash Point

100.0 °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 Tert-butyl (R)-(4-chlorobutan-2-YL)carbamate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Avoid inhalation, ingestion, and skin contact. In case of exposure, refer to the Safety Data Sheet (SDS) for specific first-aid measures. Store in a cool, dry place, away from incompatible materials. This compound is for research use only and not for human or animal therapeutic or diagnostic use.

Related Products / Graph Discovery

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

Similar products (text references)

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Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 292419GHS Pictograms: GHS07Shipment review: Shipment details require review before fulfillment.

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