Description

Carbamic Acid, (2-Hydroxy-2-Propenyl)-, 1,1-Dimethylethyl Ester (9Ci) is a specialized organic compound with a CAS number of 208935-50-6, serving as a valuable building block in advanced organic synthesis. Its molecular structure, featuring both a carbamate and a reactive allylic alcohol moiety, makes it a versatile intermediate for constructing more complex molecules. This compound is primarily sought by research and development chemists in the pharmaceutical and agrochemical industries for the synthesis of novel active ingredients and functional materials.

Application

This chemical intermediate is designed for sophisticated synthetic applications where precise molecular construction is required.

• Pharmaceutical Intermediate: A key precursor in the research and development of new active pharmaceutical ingredients (APIs), particularly for compounds requiring carbamate or allylic functional groups.
• Agrochemical Synthesis: Used in the development of novel herbicides, fungicides, and insecticides, where its reactive sites allow for the creation of targeted bioactive molecules.
• Polymer Science: Acts as a functional monomer or cross-linking agent in the synthesis of specialty polymers with tailored properties, such as polyurethanes or coatings.
• Chemical Research: Employed in academic and industrial R&D laboratories for methodological studies, catalysis research, and the exploration of new reaction pathways.
• Fine Chemical Production: Serves as a building block for the manufacture of complex dyes, pigments, and other high-value specialty chemicals.

Basic Information

Product Name	Carbamic Acid, (2-Hydroxy-2-Propenyl)-, 1,1-Dimethylethyl Ester (9Ci)
CAS No.	208935-50-6
Molecular Formula	C8H15NO3
Molecular Weight	173.21 g/mol
Synonyms	tert-Butyl N-(2-hydroxyallyl)carbamate; 1,1-Dimethylethyl N-(2-hydroxy-2-propenyl)carbamate; tert-Butyl (2-hydroxyallyl)carbamate; N-(2-Hydroxyallyl)carbamic Acid tert-Butyl Ester; (2-Hydroxyallyl)carbamic Acid tert-Butyl Ester; tert-Butoxycarbonyl-(2-hydroxyallyl)amine; BOC-N-(2-hydroxyallyl)amine; Allyl alcohol, 2-[(tert-butoxycarbonyl)amino]-
EINECS	Contact for details

Quality Control

We maintain a rigorous quality management system to ensure batch-to-batch consistency and purity for research and industrial use. Our products undergo comprehensive analytical testing, including HPLC, GC, NMR, and IR spectroscopy, to verify identity and assay. A Certificate of Analysis (COA) detailing purity, physical characteristics, and impurity profiles is provided with every shipment and is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Keep away from heat, sparks, and open flame. Due to its light-sensitive nature, containers should be amber-colored or stored in dark conditions.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

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