62521-42-0

Basic information

• Product Name: Oxazole, 4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-
• CAS NO: 62521-42-0
• Molecular Formula: C9H11NOS
• Molecular Weight: 181.258
• Mol File: 62521-42-0.mol

Chemical Properties

• CAS DataBase Reference: Oxazole, 4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Oxazole, 4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-(62521-42-0)
• EPA Substance Registry System: Oxazole, 4,5-dihydro-4,4-dimethyl-2-(2-thienyl)-(62521-42-0)

Safety Data

• Hazardous Substances Data: 62521-42-0(Hazardous Substances Data)

Upstream product

• 1003-31-2 thiophene-2-carbonitrile 
• 124-68-5 2-Amino-2-methyl-1-propanol 

Downstream Products

• 62521-44-2 2-<3-(α-Hydroxybenzyl)-2-thienyl>-4,4-dimethyl-2-oxazolin 
• 62521-43-1 [5-(4,4-dimethyl-4,5-dihydro-oxazol-2-yl)-thiophen-2-yl]-phenyl-methanol 
• 128608-98-0 4,4-dimethyl-2-(3-phenyl-2-thienyl)oxazoline 
• 527-72-0 2-thiophenylcarboxylic acid 
• 45753-18-2 2-(thiophen-2-yl)-4,5-dihydro-1H-imidazole 
• 167770-27-6 4,5-dihydro-4,4-dimethyl-2-[3-[(2-nitrophenyl)methyl]-thien-2-yl]oxazole 
• 154385-66-7 {2-(4,4-dimethyl-2-oxazolinyl)-3-thienyl}tri(phenyl)tin 
• 154385-69-0 {2-(4,4-dimethyl-2-oxazolinyl)-3-thienyl}tri(cyclohexyl)tin 
• 154385-67-8 {2-(4,4-dimethyl-2-oxazolinyl)-3-thienyl}tri(p-chlorophenyl)tin 
• 154385-65-6 {2-(4,4-dimethyl-2-oxazolinyl)-3-thienyl}tri(p-tolyl)tin 
• 154385-71-4 bis{2-(4,4-dimethyl-2-oxazolinyl)-3-thienyl}di(p-tolyl)tin 
• 113615-94-4 C₂₂H₂₄N₂O₃S 
• 97759-90-5 3-trimethylsilylthiophene-2-carboxylic acid 
• 1451-95-2 thiophene-2,3-dicarboxylic acid 

Relevant articles and documents

A general and convenient route to oxazolyl ligands

A diverse range of chiral and achiral oxazolyl ligands, which have many applications including catalysis and luminescent devices, are synthesized simply in three steps from readily available and inexpensive phenol and amino alcohol starting materials. The method can be applied to ligands with electron-donating/-withdrawing and sterically demanding/undemanding substituents, and can conveniently be scaled up to >25 g of product.

A novel and chemoselective synthesis of 2-aryloxazolines and bis-oxazolines catalyzed by Bi(III) salts

Different arylnitriles react with β-aminoalcohols in the presence of catalytic amounts of Bi(III) salts such as Bi(TFA)3, Bi(OTf) 3 and BiOClO4·XH2O producing the corresponding 2-aryl-oxazolines in high yields. Selective synthesis of mono- and bis-oxazolines from dicyanobenzenes and selective conversion of arylnitriles to their 2-oxazolines in the presence of alkylnitriles can be considered as noteworthy advantages of this method. Georg Thieme Verlag Stuttgart.