184429-84-3

Basic information

• Product Name: Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate
• Synonyms: Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate;tert-Butyl (3-((tert-butyldimethylsilyl)oxy)-2-oxopropyl)carbamate
• CAS NO: 184429-84-3
• Molecular Formula: C₁₄H₂₉NO₄Si
• Molecular Weight: 303.46986
• Mol File: 184429-84-3.mol

Chemical Properties

• Boiling Point: 347.5±27.0 °C(Predicted)
• Appearance: /
• Density: 0.975±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 10.85±0.46(Predicted)
• CAS DataBase Reference: Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate(184429-84-3)
• EPA Substance Registry System: Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate(184429-84-3)

Safety Data

• Hazardous Substances Data: 184429-84-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate is used as a protecting group for alcohols in organic synthesis to facilitate selective reactions without affecting the alcohol moiety.
Used in Chemical Research:
In the field of chemical research, Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate is utilized for the manipulation and functionalization of alcohol groups in complex molecule synthesis, providing stability and protection to the alcohol functional group.
Used in Pharmaceutical Industry:
Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate is used as a key intermediate in the synthesis of pharmaceutical compounds, aiding in the development of new drugs by protecting alcohol groups during the synthesis process.
Used in Material Science:
In material science, Tert-Butyl N-(3-[(Tert-Butyldimethylsilyl)Oxy]-2-Oxopropyl)Carbamate is employed in the synthesis of advanced materials, where the protection of alcohol groups is essential for creating complex molecular structures with specific properties.

Upstream product

• 137618-48-5 tert-butyl N-(2,3-dihydroxypropyl)carbamate 

Relevant articles and documents

Allylamine derivative as well as preparation method and application thereof

The invention relates to an allylamine derivative as well as a preparation method and application thereof, and in particular, relates to a compound represented by a formula I, or a stereoisomer, a tautomer, a polymorphic substance, a solvate, an N-oxide, an isotope labeled compound, a metabolite, a prodrug or ester thereof, or a pharmaceutically acceptable salt thereof. The compound has a higher inhibitory activity against vascular adhesion protein 1/semicarbazide sensitive amine oxidase, a good selectivity against monoamine oxidase and diamine oxidase; and additionally, in some embodiments, the mixture has a high in vivo bioavailability as well as safety.

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VASCULAR ADHESION PROTEIN-1 (VAP-1) MODULATORS AND THERAPEUTIC USES THEREOF

Disclosed herein are small molecule Vascular Adhesion Protein- 1 (VAP-1) modulator compositions, pharmaceutical compositions, the use and preparation thereof.

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SSAO INHIBITORS AND USES THEREOF

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