15833-64-4

Basic information

• Product Name: 3-Furanmethanol, tetrahydro-3-methyl-
• CAS NO: 15833-64-4
• Molecular Formula: C6H12O2
• Molecular Weight: 116.16
• Mol File: 15833-64-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-Furanmethanol, tetrahydro-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Furanmethanol, tetrahydro-3-methyl-(15833-64-4)
• EPA Substance Registry System: 3-Furanmethanol, tetrahydro-3-methyl-(15833-64-4)

Safety Data

• Hazardous Substances Data: 15833-64-4(Hazardous Substances Data)

Upstream product

• 1445651-64-8 tetrahydro-furan-3-carboxylic acid benzyl ester 
• 89364-31-8 3-tetrahydrofuroic acid 
• 88214-48-6 3-(2-hydroxyethyl)-3-methyloxetane 
• 7459-46-3 triethyl 1,1,2-ethanetricarboxylate 
• 119117-07-6 2-(hydroxymethyl)-2-methylbutane-1,4-diol 
• 39994-45-1 triethyl propane-1,2,2-tricarboxylate 

Relevant articles and documents

ALKYNYL QUINAZOLINE COMPOUNDS

The present disclosure relates to compounds of Formula (I'): and pharmaceutically acceptable salts and stereoisomers thereof. The present disclosure also relates to methods of preparation these compounds, compositions comprising these compounds, and methods of using them in the prevention or treatment of abnormal cell growth in mammals, especially humans.

3-(1H-PYRAZOL-4-YL)PYRIDINE ALLOSTERIC MODULATORS OF THE M4 MUSCARINIC ACETYLCHOLINE RECEPTOR

The present invention is directed to pyrazol-4-yl-pyridine compounds which are allosteric modulators of the M4 muscarinic acetylcholine receptor. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which M4 muscarinic acetylcholine receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which M4 muscarinic acetylcholine receptors are involved.

Enantioselective intramolecular openings of oxetanes catalyzed by (salen)Co(lll) complexes: Access to enantioenriched tetrahydrofurans

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