182629-25-0

Basic information

• Product Name: 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dimethanol
• Synonyms: 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dimethanol
• CAS NO: 182629-25-0
• Molecular Weight: 268.428
• Mol File: 182629-25-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dimethanol(182629-25-0)
• EPA Substance Registry System: 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dimethanol(182629-25-0)

Safety Data

• Hazardous Substances Data: 182629-25-0(Hazardous Substances Data)

Upstream product

• 618-83-7 5-Hydroxyisophthalic acid 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 182629-24-9 dimethyl 5-{[(1,1-dimethylethyl)dimethylsilyl]oxy}benzene-1,3-dicarboxylate 
• 219965-98-7 5-(tert-butyldimethylsilyloxy)isophthalic acid 

Downstream Products

• 685107-21-5 1-(tert-butyl-(dimethyl)-silyloxy)-3,5-bis-triisopropylsilyloxymethyl benzene 
• 1357256-05-3 methyl 3-acetyl-5-hydroxybenzoate 
• 1357256-04-2 C₁₅H₂₆O₃Si 
• 1357255-99-2 3'-(tert-butyldimethylsilyl)oxy-5'-(3-hydroxypentan-3-yl)acetophenone 
• 1357255-98-1 3'-(methoxymethoxy)-5'-(3-hydroxypentan-3-yl)acetophenone 
• 1357256-01-9 methyl 3-acetyl-5-{(tert-butyldimethylsilyl)oxy}benzoate 
• 1357256-00-8 methyl 3-acetyl-5-(methoxymethoxy)benzoate 
• 182629-21-6 1,3-bis(dimethylaminomethyl)-5-((tert-butyldimethylsilyl)oxy)benzene 
• 186605-76-5 3,5-bis[3,5-bis(methoxycarbonyl)phenoxymethyl]phenol 
• 194864-27-2 3,5-Bis-tert-butylsulfanylmethyl-phenol 
• 194864-28-3 3,5-Bis-ethylsulfanylmethyl-phenol 
• 168414-91-3 [3,5-Bis-(3,5-bis-phenylsulfanylmethyl-phenoxymethyl)-phenyl]-acetonitrile 
• 350025-97-7 1-[3-(tert-butyl-dimethyl-silanyloxy)-5-(1-hydroxy-propyl)-phenyl]-propan-1-ol 

Relevant articles and documents

Linked bis-isophthalic acid derivatives as building blocks in the design of self-assembling structures

In this paper we show that linked bis-isophthalic acid derivatives form ordered molecular structures in the solid state. The key organizing interactions are hydrogen bonds between the isophthalate carboxylic acid substituents on adjacent molecules or to methanol solvent. NMR investigations suggest that alternative aggregates form in solution.

NITRIC OXIDE RELEASING SELECTIVE CYCLOOXYGENASE-2 INHIBITORS

The invention encompasses novel compounds of Formula (I) and Formula (II), which are nitric oxide-releasing prodrugs useful in the treatment of cyclooxygenase-2 mediated diseases. The invention also encompasses certain pharmaceutical compositions and meth

Supramolecular side-chain functionalized polymers: Synthesis and self-assembly behavior of polynorbornenes bearing PdII SCS pincer complexes

A new polynorbornene bearing palladated SCS pincer complexes at each repeat unit has been synthesized using ring-opening metathesis polymerization. Small mesogenic molecules possessing nitrile or pyridine-based anchoring units are instantaneously and quantitatively coordinated to the palladium center in one simple self-assembly step giving rise to a densely functionalized polymer. These results suggest that the coordination of mesogenic small molecules onto the polymer scaffold can provide a simple and efficient route to a variety of materials.