249937-07-3

Basic information

• Product Name: (3-BROMOPHENETHOXY)(TERT-BUTYL)DIMETHYLSILANE
• Synonyms: 3-[2-(T-BUTYLDIMETHYLSILYLOXY)ETHYL]-1-BROMOBENZENE;(3-BROMOPHENETHOXY)(TERT-BUTYL)DIMETHYLSILANE;1-Bromo-3-[2-(tert-butyldimethylsilyloxy)ethyl]benzene;1-Bromo-3-[2-(tert-butyldimethylsilyloxy)ethyl]benzene 98%;1-Bromo-3-[2-(tert-butyldimethylsilyloxy)ethyl]benzene98%
• CAS NO: 249937-07-3
• Molecular Formula: C₁₄H₂₃BrOSi
• Molecular Weight: 315.32132
• Product Categories: blocks;Bromides
• Mol File: 249937-07-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 317.782 °C at 760 mmHg
• Flash Point: 145.99 °C
• Appearance: /
• Density: 1.128 g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.496
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (3-BROMOPHENETHOXY)(TERT-BUTYL)DIMETHYLSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: (3-BROMOPHENETHOXY)(TERT-BUTYL)DIMETHYLSILANE(249937-07-3)
• EPA Substance Registry System: (3-BROMOPHENETHOXY)(TERT-BUTYL)DIMETHYLSILANE(249937-07-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 249937-07-3(Hazardous Substances Data)

Usage

General Description

(3-BROMOPHENETHOXY)(tert-butyl)dimethylsilane is a specific chemical compound with the formula C14H23BrOSi. It is a silane compound containing a bromophenethoxy group and a tert-butyl group attached to a silicon atom. Silane compounds are commonly used as coupling agents to improve the adhesion between organic polymers and inorganic materials. This particular compound may find applications in organic synthesis and materials science due to its unique reactivity and properties. It should be handled with care and in accordance with proper safety precautions due to its potential hazards and reactivity.

InChI:InChI=1/C14H23BrOSi/c1-14(2,3)17(4,5)16-10-9-12-7-6-8-13(15)11-12/h6-8,11H,9-10H2,1-5H3

Upstream product

• 1878-67-7 3-Bromophenylacetic acid 
• 28229-69-8 2-(3-bromophenyl)ethan-1-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 1298046-66-8 toluene-4-sulfonic acid 2-(3-oxetan-3-yl-phenyl)-ethyl ester 
• 1298046-65-7 2-(3-oxetan-3-yl-phenyl)-ethanol 
• 1298046-64-6 tert-butyl-dimethyl-[2-(3-oxetan-3-yl-phenyl)-ethoxy]-silane 
• 604768-85-6 3-(2-(tert-butyl)dimethylsilyloxyethyl)phenylboronic acid 
• 249937-10-8 methanesulfonic acid 2-{3-[5-amino-1-(4-fluorophenyl)-1H-pyrazole-4-carbonyl]phenyl}ethyl ester 
• 249937-11-9 5-amino-1-(4-fluorophenyl)-4-[3-(2-azidoethyl)benzoyl]pyrazole 
• 249936-65-0 [5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl][3-(2-hydroxyethyl)phenyl]-methanone 
• 249937-09-5 5-amino-1-(4-fluorophenyl)-4-[3-(2-tert-butyldimethylsilyloxyethyl)benzoyl]pyrazole 
• 647853-32-5 (3-(2-hydroxyethyl)phenyl)boronic acid 
• 882695-37-6 4-[3-(2-Hydroxy-ethyl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

ANTIMICROBIAL COMPOUNDS AND METHODS

The invention is directed to compounds that are active as antibacterial agents. The invention compounds are active against gram-positive and gram-negative bacteria and can be used to treat infections caused by gram-positive and gram-negative bacteria. Also disclosed are processes and intermediates for making the compounds.

Design and synthesis of novel meta-linked phenylglycine macrocyclic FVIIa inhibitors

Two novel series of meta-linked phenylglycine-based macrocyclic FVIIa inhibitors have been designed to improve the rodent metabolic stability and PK observed with the precursor para-linked phenylglycine macrocycles. Through iterative structure-based design and optimization, the TF/ FVIIa Ki was improved to subnanomolar levels with good clotting activity, metabolic stability, and permeability.

Photochemistry of acyloximes: Synthesis of heterocycles and natural products

New applications of the photochemically generated iminyl radicals ring closure onto phenyl, thiophenyl, and pyridinyl rings are presented. The influence on the reactivity of different substituent throughout the acyloxime structure is discussed. Some obser