82977-45-5

Basic information

• Product Name: 2-Furancarbonyl chloride, tetrahydro-5-oxo- (9CI)
• Synonyms: 2-Furancarbonyl chloride, tetrahydro-5-oxo- (9CI)
• CAS NO: 82977-45-5
• Molecular Formula: C₅H₅ClO₃
• Molecular Weight: 148.5444
• Product Categories: ACIDHALIDE
• Mol File: 82977-45-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Furancarbonyl chloride, tetrahydro-5-oxo- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Furancarbonyl chloride, tetrahydro-5-oxo- (9CI)(82977-45-5)
• EPA Substance Registry System: 2-Furancarbonyl chloride, tetrahydro-5-oxo- (9CI)(82977-45-5)

Safety Data

• Hazardous Substances Data: 82977-45-5(Hazardous Substances Data)

Upstream product

• 617-65-2 Glutamic acid 
• 4344-84-7 5-oxo-tetrahydro-furan-2-carboxylic acid 

Downstream Products

• 1402054-40-3 ethyl 2-(4-(4-(2-(6-amino-4-(2-(5-oxotetrahydrofuran-2-carbonyl)hydrazinyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)ethyl)piperazin-1-yl)phenoxy)acetate 
• 433960-48-6 tert-butyl 2-amino-6-(2-hydroxyphenyl)-4-(3-{[(5-oxotetrahydro-2-furanyl)carbonyl]amino}-phenyl)-nicotinate 
• 433957-83-6 N-{3-[2-amino-3-cyano-6-(2-hydroxyphenyl)-4-pyridinyl]phenyl}-5-oxotetrahydro-2-furancarboxamide 
• 433958-69-1 5-oxo-tetrahydro-furan-2-carboxylic acid {3-[2-amino-3-cyano-6-(2-hydroxy-6-methoxy-phenyl)-pyridin-4-yl]-phenyl}-amide 

Relevant articles and documents

STAT DEGRADERS AND USES THEREOF

The present invention provides compounds, compositions thereof, and methods of using the same.

METABOLITES OF 2-(FURAN-2-YL)-7-(2-(4-(4-(2-METHOXYETHOXY)PHENYL)PIPERAZIN-1-YL)ETHYL)-7H-PYRAZOLO[4,3-e][1,2,4]TRIAZOLO[1,5-c]PYRIMIDIN-5-AMINE AND THEIR UTILITY AS ADENOSINE A2a RECEPTOR ANTAGONISTS

The present invention provides a compound of the (formula:(I) or a pharmaceutically acceptable salt thereof in isolated and purified form. The compound is an adenosine A2a receptor antagonists useful in treatment of central nervous system disorders, such

Haem d1: Development of a new coupling procedure leading to the synthesis of isobacteriochlorins

A new approach has been developed for construction of the western and eastern lactams, e.g. 2 and 3, needed for synthesis of isobacteriochlorins. It involves acylation of pyrroles with lactonic acids to form ketones. These are then efficiently converted into the desired lactams by a short sequence of reactions. All the steps are high yielding and simple to carry out.