195197-94-5

Basic information

• Product Name: tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate
• Synonyms: tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate;TERT-BUTYL N-(3-[(TERT-BUTYLDIMETHYLSILYL)OXY]-2-HYDROXYPROPYL)CARBAMATE;[3-(tert-Butyldimethylsilanyloxy)-2-hydroxypropyl]carbamic acid tert-butyl ester;TERT-BUTYL N-(3-[(TERT-BUTYLDIMETHYLSILYL)OXY]-2-HYDROXYPROPYL)CARBAMATE(WX642128)
• CAS NO: 195197-94-5
• Molecular Formula: C₁₄H₃₁NO₄Si
• Molecular Weight: 305.49
• Mol File: 195197-94-5.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate(195197-94-5)
• EPA Substance Registry System: tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate(195197-94-5)

Safety Data

• Hazardous Substances Data: 195197-94-5(Hazardous Substances Data)

Usage

General Description

Tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate is a compound consisting of a tert-butyl group, a tert-butyldimethylsilyloxy group, and a carbamate group attached to a 2-hydroxypropyl chain. tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate is commonly used as a protecting group in organic synthesis to prevent undesired side reactions or to protect certain functional groups during chemical reactions. It is known for its stability and ability to be easily removed under mild conditions, making it a valuable tool in chemical synthesis. Additionally, the tert-butyldimethylsilyloxy group provides increased lipophilicity, which can be beneficial in certain applications. Overall, tert-butyl 3-(tert-butyldimethylsilyloxy)-2-hydroxypropylcarbamate is a versatile chemical compound with various applications in organic chemistry.

Upstream product

• 137618-48-5 tert-butyl N-(2,3-dihydroxypropyl)carbamate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 34619-03-9 tert-butyldicarbonate 

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.

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.

SSAO INHIBITOR

The present invention provides an SSAO inhibitor and an application thereof in preparing a drug for treating a disease related to SSAO. In particular, the present invention provides a compound shown in formula (IV) and a pharmaceutically acceptable salt thereof.