139232-40-9

Basic information

• Product Name: IRFI 005
• Synonyms: IRFI 005
• CAS NO: 139232-40-9
• Molecular Formula: C13H16O4
• Molecular Weight: 236.26374
• Mol File: 139232-40-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 459°C at 760 mmHg
• Flash Point: 178.6°C
• Appearance: /
• Density: 1.249g/cm³
• Vapor Pressure: 3.2E-09mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: IRFI 005(CAS DataBase Reference)
• NIST Chemistry Reference: IRFI 005(139232-40-9)
• EPA Substance Registry System: IRFI 005(139232-40-9)

Safety Data

• Hazardous Substances Data: 139232-40-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H16O4/c1-6-7(2)13-10(8(3)12(6)16)4-9(17-13)5-11(14)15/h9,16H,4-5H2,1-3H3,(H,14,15)

Upstream product

• 1049661-94-0 (E)-4-(2,5-Dihydroxy-3,4,6-trimethyl-phenyl)-but-2-enoic acid methyl ester 

Downstream Products

• 134867-64-4 methyl (+/-)-5-benzyloxy-2,3-dihydro-4,6,7-trimethyl-2-benzofuranacetate 
• 134867-67-7 N-[2-(2,3-dihydro-5-benzyloxy-4,6,7-trimethyl-2-benzofuranyl)ethyl]phthalimide 
• 134867-68-8 (+/-)-5-benzyloxy-2,3-dihydro-4,6,7-trimethyl-2-benzofuranethanol p-toluenesulfonate 
• 154954-48-0 (+/-)-2,3-dihydro-5-(2-methoxyethoxymethoxy)-4,6,7-trimethyl-2-<2-(p-nitrophenyloxy)ethyl>benzofuran 
• 134867-34-8 (+/-)-5-benzyloxy-2,3-dihydro-4,6,7-trimethyl-2-benzofuranethanamine 
• 134867-29-1 (+/-)-5-benzyloxy-2,3-dihydro-4,6,7-trimethyl-2-benzofuranethanol 
• 134867-38-2 (+/-)-2-(2-bromoethyl)-5-benzyloxy-2,3-dihydro-4,6,7-trimethylbenzofuran 
• 134867-37-1 (+/-)-5-benzyloxy-2-ethyl-2,3-dihydro-4,6,7-trimethylbenzofuran 

Relevant articles and documents

A powerful hydrogen-bond-donating organocatalyst for the enantioselective intramolecular oxa-michael reaction of α,β-unsaturated amides and esters

Tuning the organocatalyst: An unprecedented enantioselective intramolecular oxa-Michael reaction of unactivated α,β-unsaturated amides and esters catalyzed by a powerful hydrogen-bond-donating organocatalyst has been developed. Furthermore, the products obtained from this reaction have been used for the straightforward asymmetric synthesis of several natural products and biologically important compounds. Copyright

(RS)-2-(2,3-dihydro-5-hydroxy-4,6,7-trimethylbenzofuranyl) acetic acids and 2-(2,3-dihydro-5-acyloxy-4,6,7-trimethylbenzofuranyl) acetic acids and esters thereof, useful as mucoregulator and anti-ischemic drugs

The present invention relates to (RS)-2-(2,3-dihydro-5-hydroxy-4,6,7-trimethylbenzofuranyl) acetic acids and 2-(2,3-dihydro-5-acyloxy-4,6,7-trimethylbenzofuranyl) acetic acids and esters thereof, the process for producing them and their relevant therapeut