96013-79-5

Basic information

• Product Name: Benzenemethanol, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-
• CAS NO: 96013-79-5
• Molecular Formula: C13H22O2Si
• Molecular Weight: 238.402
• Mol File: 96013-79-5.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-(96013-79-5)
• EPA Substance Registry System: Benzenemethanol, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-(96013-79-5)

Safety Data

• Hazardous Substances Data: 96013-79-5(Hazardous Substances Data)

Upstream product

• 90-01-7 salicylic alcohol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 82112-31-0 1-(tert-butyldimethylsilanyloxy)-2-(tert-butyldimethylsilanyloxymethyl)benzene 

Downstream Products

• 39894-71-8 3-(2-hydroxyphenyl)propyne 
• 1007587-65-6 2-(trimethylsilylethynylmethyl)phenyl tert-butyldimethylsilyl ether 
• 82112-31-0 1-(tert-butyldimethylsilanyloxy)-2-(tert-butyldimethylsilanyloxymethyl)benzene 
• 63449-79-6 4-(o-methoxyphenyl)-butan-2-one 
• 61844-32-4 4-(2-hydroxyphenyl)butan-2-one 

Relevant articles and documents

PROBE FOR DETECTING CARBAPENEM-RESISTANT BACTERIA AND USE THEREOF

The present disclosure relates to a compound represented by Chemical Formula 1, a probe for detecting antibiotic-resistant bacteria, which includes the compound, a composition containing the compound, a kit including the compound and a method for detectin

Hafnium Triflate as a Highly Potent Catalyst for Regio- and Chemoselective Deprotection of Silyl Ethers

As a Group IVB transition metal Lewis acid, hafnium triflate [Hf(OTf) 4 ] exhibited exceptionally high potency in desilylations. Since the amounts of Hf(OTf) 4 required for the deprotection of 1°, 2°, 3° alkyl and aryl tert -butyldimethylsilyl (TBS) ethers are significantly different, ranging from 0.05 mol% to 3 mol%, regioselective deprotection of TBS could be easily implemented. Moreover, chemoselective cleavage of different silyl ethers or removal of TBS in the presence of most hydroxyl protecting groups was also accomplished. NMR analyses of silyl products from TBS deprotection indicated that Hf(OTf) 4 -catalyzed desilylation may proceed via different mechanisms, depending on the solvent used.

PRODRUGS OF FUSED-BICYCLIC C5aR ANTAGONISTS

The present disclosure provides, inter alia, Compounds of Formulae IA, IB, IC, IIA, IIB and IIC or pharmaceutically acceptable salts thereof that are modulators of the C5a receptor. Also provided are pharmaceutical compositions and methods of use including the treatment of diseases or disorders involving pathologic activation from C5a and non-pharmaceutical applications.