Description

tert-Butyl n-[(E)-3-Tributylstannylallyl]Carbamate is a specialized organotin reagent featuring a protected amine group. This compound matters as a versatile building block in advanced organic synthesis, enabling the controlled introduction of the allylstannane moiety for cross-coupling and radical reactions. It is primarily needed by R&D chemists and process development teams in the pharmaceutical, agrochemical, and advanced materials industries for constructing complex molecular architectures.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of active pharmaceutical ingredients (APIs), particularly for introducing functionalized allyl groups via Stille coupling.
• Agrochemical Synthesis: Used in the research and development of novel pesticides and herbicides where precise carbon-tin bond transformations are required.
• Material Science Research: Serves as a monomer or functionalization agent in the development of polymers and advanced organic materials with tailored properties.
• Cross-Coupling Reactions: An essential reagent for Pd-catalyzed Stille cross-coupling reactions to form new carbon-carbon bonds in complex molecule assembly.
• Radical Chemistry: Acts as a source of allyl radicals in tin-mediated radical chain reactions for stereoselective synthesis.
• Organic Methodology Development: Used in academic and industrial labs to develop new synthetic methodologies involving organometallic chemistry.

Basic Information

Product Name	tert-Butyl n-[(E)-3-Tributylstannylallyl]Carbamate
CAS No.	139111-44-7
Molecular Formula	C₂₀H₄₁NO₂Sn
Molecular Weight	446.26 g/mol
Synonyms	Boc-Protected 3-(Tributylstannyl)allylamine; tert-Butyl (E)-3-(tributylstannyl)allylcarbamate; (E)-tert-Butyl (3-(tributylstannyl)allyl)carbamate; N-Boc-3-(tributylstannyl)allylamine; 3-(Tributylstannyl)allyl tert-butyl carbamate; Allyltributylstannane, N-Boc protected; tert-Butyl N-[(1E)-3-(tributylstannyl)-2-propen-1-yl]carbamate
EINECS	Contact for details

Quality Control

Our tert-Butyl n-[(E)-3-Tributylstannylallyl]Carbamate undergoes rigorous quality testing to ensure compliance with industry standards for research and process chemistry. Each batch is characterized by NMR (¹H, ¹³C), FT-IR, and HPLC analysis to confirm identity, isomeric purity (E-configuration), and chemical purity. Certificates of Analysis (COA) with full analytical data are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) at 2-8°C to minimize oxidation and degradation. Keep the container in a cool, dry, well-ventilated place, away from incompatible materials.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 95% (Area %)
Isomeric Purity (E-isomer)	≥ 98%
Tin (Sn) Content	Theoretical ~26.6%

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