38453-94-0

Basic information

• Product Name: ETHYL 5-(TERT-BUTYL)-2-METHYL-3-FUROATE
• Synonyms: ETHYL 5-(TERT-BUTYL)-2-METHYL-3-FUROATE;Ethyl 5-(tert-butyl)-2-methylfuran-3-carboxylate
• CAS NO: 38453-94-0
• Molecular Formula: C₁₂H₁₈O₃
• Molecular Weight: 210.27
• Mol File: 38453-94-0.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ETHYL 5-(TERT-BUTYL)-2-METHYL-3-FUROATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 5-(TERT-BUTYL)-2-METHYL-3-FUROATE(38453-94-0)
• EPA Substance Registry System: ETHYL 5-(TERT-BUTYL)-2-METHYL-3-FUROATE(38453-94-0)

Safety Data

• Hazardous Substances Data: 38453-94-0(Hazardous Substances Data)

Upstream product

• 28921-35-9 2-methyl-3-ethoxycarbonyl-furan 
• 507-19-7 t-butyl bromide 
• 38453-93-9 ethyl 2-acetyl-5,5-dimethyl-4-oxopentanoate 
• 2303-76-6 sodium diethyl phosphite 
• 13547-70-1 1-chloro-3,3-dimethyl-butan-2-one 
• 92975-23-0 (Z)-2,2-Dimethyl-5-trimethylsilanyloxy-hex-4-en-3-one 
• 7307-04-2 acetylpinacolin 
• 141-97-9 ethyl acetoacetate 
• 5469-26-1 1-Bromopinacolon 
• 1007476-32-5 sodium ethyl acetylacetate enolate 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 2009-97-4 ethyl 2-diazo-3-oxobutanoate 
• 2987-16-8 3,3-dimethylbutyrylaldehyde 

Downstream Products

• 38422-62-7 5-(tert-butyl)-2-methylfuran-3-carboxylic acid 
• 502990-82-1 2-methyl-4-chloromethyl-5-tert-butylfuran-3-carboxylic acid chloride 
• 154160-54-0 (5-tert-Butyl-2-methyl-3-furyl)methyl benzoate 
• 908239-56-5 C₃₀H₂₈NO₂P 

Relevant articles and documents

Auto-Tandem Catalysis-Induced Synthesis of Trisubstituted Furans through Domino Acid-Acid-Catalyzed Reaction of Aliphatic Aldehydes and 1,3-Dicarbonyl Compounds by using N-Bromosuccinimide as Oxidant

A simple aluminium(III) chloride-catalyzed synthesis of tri-substituted furans from aliphatic aldehydes and 1,3-dicarbonyl compounds was developed by using N-bromosuccinimide (NBS) as an oxidant. This method was effective for the synthesis of various furan derivatives. Some of the products were not accessible with the previously reported methods. Mechanically, this reaction involved an auto-tandem catalysis based on a newly reported acid-acid-catalyzed tandem reaction to ensure that furans were successfully synthesized. (Figure presented.).

Cu(I)-catalyzed reaction of diazo compounds with terminal alkynes: A direct synthesis of trisubstituted furans

A method for the synthesis of tri-substituted furans has been developed based on Cu(I)-catalyzed reaction of terminal alkynes with β-keto α-diazoesters. This method for the synthesis of 2,3,5-trisubstituted furans is operationally simple and applicable to

HETEROCYCLIC COMPOUND

The present invention provides a heterocyclic compound represented by the following formula (I), which has a glucagon antagonistic action and is useful for the prophylaxis or treatment of diabetes and the like, a compound represented by wherein ring A is an optionally substituted benzene ring and the like; Y is a nitrogen atom and the like; X is -O- and the like; R4 is a hydrogen atom and the like; R5 and R6 are each independently a hydrogen atom and the like; R1 is an optionally substituted hydrocarbon group and the like; R2 is a hydrogen atom and the like; and R3 is -(CH2)3-COOH and the like, or a salt thereof.