Description

Carbamic Acid, (2,2-Dimethoxy-1-Methylethyl)-, 1,1-Dimethylethyl Ester, (R)- is a high-purity, chiral carbamate derivative of significant value in advanced organic synthesis. This compound serves as a critical chiral building block and protecting group intermediate, enabling the stereoselective construction of complex molecules. It is primarily sought after by research institutions and pharmaceutical manufacturers engaged in the development of novel active pharmaceutical ingredients (APIs) and fine chemicals.

Application

• Pharmaceutical Intermediate: A key chiral synthon in the multi-step synthesis of potential drug candidates, particularly in medicinal chemistry research.
• Asymmetric Synthesis: Utilized as a chiral auxiliary or reagent in stereocontrolled chemical reactions to introduce specific stereochemistry.
• Amino Acid & Peptide Chemistry: Acts as a protecting group for amines during the synthesis of complex peptides and modified amino acid derivatives.
• Agrochemical Research: Employed in the development of chiral active ingredients for crop protection products.
• Academic & Process R&D: Used in laboratory-scale research and process development for route scouting and optimization.
• Fine Chemical Production: Incorporated into the manufacture of specialty chemicals requiring high enantiomeric purity.

Basic Information

Product Name	Carbamic Acid, (2,2-Dimethoxy-1-Methylethyl)-, 1,1-Dimethylethyl Ester, (R)-
CAS No.	194094-87-6
Molecular Formula	C12H25NO4
Molecular Weight	247.33 g/mol
Synonyms	(R)-tert-Butyl (2,2-dimethoxy-1-methylethyl)carbamate; (R)-N-Boc-2,2-dimethoxy-1-methylethylamine; (R)-1,1-Dimethylethyl N-(2,2-dimethoxy-1-methylethyl)carbamate; (R)-Boc-Amidine acetal; (R)-tert-Butyl (1-(dimethoxymethyl)ethyl)carbamate; (R)-N-(tert-Butoxycarbonyl)-2,2-dimethoxy-1-methylethylamine; (R)-Boc-Protected amidine acetal
EINECS	Contact for details

Quality Control

Our production of Carbamic Acid, (2,2-Dimethoxy-1-Methylethyl)-, 1,1-Dimethylethyl Ester, (R)- adheres to stringent internal quality standards to ensure batch-to-batch consistency and high enantiomeric purity. Each lot is characterized by advanced analytical techniques including chiral HPLC, NMR, and GC/MS. Certificates of Analysis (COA) detailing identity, purity, and chiral excess are provided with every shipment to support your quality and regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from strong acids and incompatible organic solvents. For long-term storage, consider maintaining the material under an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 98.0% ee
Water Content (KF)	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.