Description

Carbamic Acid, n-1-Oxaspiro[2.5]Oct-6-Yl-, 1,1-Dimethylethyl Ester is a specialized spirocyclic carbamate derivative, serving as a high-value synthetic intermediate in advanced organic synthesis. Its unique molecular architecture, featuring a fused oxaspiro ring system, makes it a critical building block for constructing complex pharmacophores and fine chemicals. This compound is essential for R&D and production chemists in the pharmaceutical and agrochemical sectors, where it is utilized to develop novel active ingredients and functional materials.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of novel drug candidates, particularly those targeting central nervous system (CNS) disorders.
• Agrochemical Synthesis: Building block for developing advanced crop protection agents and herbicides with novel modes of action.
• Organic Synthesis Reagent: Used in academic and industrial research for constructing complex spirocyclic and heterocyclic compounds.
• Material Science Research: Intermediate for creating specialty polymers and advanced organic materials with specific functional properties.
• Chemical Biology Probe Development: Serves as a scaffold for designing molecular probes and enzyme inhibitors in biochemical research.

Basic Information

Product Name	Carbamic Acid, n-1-Oxaspiro[2.5]Oct-6-Yl-, 1,1-Dimethylethyl Ester
CAS No.	959704-59-7
Molecular Formula	C12H21NO3
Molecular Weight	227.30 g/mol
Synonyms	tert-Butyl N-(6-oxaspiro[2.5]oct-6-yl)carbamate; 6-[(tert-Butoxycarbonyl)amino]-6-oxaspiro[2.5]octane; 1,1-Dimethylethyl N-(6-oxaspiro[2.5]oct-6-yl)carbamate; Boc-6-oxaspiro[2.5]oct-6-yl-amine; Spiro[oxirane-2,1'-cyclopentane]-1'-methanamine, N-Boc derivative; (6-Oxaspiro[2.5]oct-6-yl)carbamic acid tert-butyl ester; tert-Butyl (6-oxaspiro[2.5]octan-6-yl)carbamate
EINECS	Contact for details

Quality Control

Our production of Carbamic Acid, n-1-Oxaspiro[2.5]Oct-6-Yl-, 1,1-Dimethylethyl Ester adheres to stringent quality management protocols. Every batch undergoes rigorous analytical testing, including HPLC, NMR, and GC-MS, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical specifications. Our quality systems are designed to support cGMP compliance for pharmaceutical applications, ensuring traceability and reliability for our global B2B partners.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This compound is hygroscopic (moisture-sensitive) and must be kept under an inert atmosphere (e.g., nitrogen or argon) in its original packaging to prevent degradation. Keep away from heat, open flames, and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (NMR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
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.