65018-90-8

Basic information

• Product Name: (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile
• Synonyms: (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile;2,2-dimethyl-2,7b-dihydro-1aH-oxireno[2,3-c]chromene-6-carbonitrile(WXG00282)
• CAS NO: 65018-90-8
• Molecular Formula: C₁₂H₁₁NO₂
• Molecular Weight: 204.24506
• Mol File: 65018-90-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile(65018-90-8)
• EPA Substance Registry System: (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile(65018-90-8)

Safety Data

• Hazardous Substances Data: 65018-90-8(Hazardous Substances Data)

Usage

General Description

The chemical compound (1aR,7aR)-7,7-diMethyl-7,7a-dihydro-1aH-oxireno[2,3-c]chroMene-3-carbonitrile, also known as oxirenochromene-3-carbonitrile, is a type of organic compound. It is a derivative of oxirenochromene, which is a class of compounds known for their potential pharmacological properties. This particular compound contains a carbonitrile functional group, which has important implications for its reactivity and potential applications. The compound's unique structure and properties make it a subject of interest for further research in the fields of medicinal chemistry and drug discovery.

Upstream product

• 33143-29-2 6-cyano-2,2-dimethylchromene 
• 94-41-7 benzalacetophenone 

Downstream Products

• 129421-83-6 trans-3,4-dihydro-4-(4-amino-1,2-dihydro-2-oxo-1-pyridyl)-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile 
• 103732-47-4 (3S,4R)-4-(4-Benzyl-2-oxo-piperazin-1-yl)-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile 
• 123596-00-9 (3S,4R)-4-(4-Benzyloxy-2-oxo-2H-pyridin-1-yl)-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile 
• 166095-21-2 BMS-191095 
• 166095-21-2 (3S,4R)-4-[(4-Chloro-phenyl)-(1H-imidazol-2-ylmethyl)-amino]-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile 
• 121055-10-5 SDZ PCO 400 
• 94470-67-4 (+/-)-cromakalim 
• 1323443-71-5 N-(6-cyano-3,4-dihydro-2,2-dimethyl-3-hydroxy-2H-1-benzopyran-4-yl)-L-tyrosine ethyl ester 
• 1323443-70-4 N-(6-cyano-3,4-dihydro-2,2-dimethyl-3-hydroxy-2H-1-benzopyran-4-yl)-L-phenylalanine ethyl ester 
• 103732-50-9 (3S,4R)-4-(4-Benzoyl-2-oxo-piperazin-1-yl)-3-hydroxy-2,2-dimethyl-chroman-6-carbonitrile 
• 108963-07-1 2-((3R,4S)-6-Cyano-3-hydroxy-2,2-dimethyl-chroman-4-yl)-N-(4-methoxy-benzyl)-N-methyl-acetamide 
• 123595-75-5 3,4-dihydro-4-(1,2-dihydro-2-oxo-1-pyridyl)-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-carbonitrile 
• 123596-08-7 trans-3,4-dihydro-3-hydroxy-2,2-dimethyl-4-(3-pyridyloxy)-2H-1-benzopyran-6-carbonitrile 
• 117545-11-6 bimakalim 

Relevant articles and documents

Asymmetric epoxidation of alkenes catalyzed by a porphyrin-inspired manganese complex

A novel strategy for catalytic asymmetric epoxidation of a wide variety of olefins by a porphyrin-inspired chiral manganese complex using H 2O2 as a terminal oxidant in excellent yield with up to greater than 99% ee has been successfully developed.

Benzopyrans

Compounds of formula (I): STR1 wherein: one of R1 and R2 is hydrogen and the other is selected from the class of alkylcarbonyl, alkoxycarbonyl, alkylcarbonyloxy, alkylhydroxymethyl, nitro, cyano, chloro, trifluoromethyl, alkylsulphin