82110-13-2

Basic information

• Product Name: (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol
• Synonyms: (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol
• CAS NO: 82110-13-2
• Molecular Weight: 116.16
• Mol File: 82110-13-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol(82110-13-2)
• EPA Substance Registry System: (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol(82110-13-2)

Safety Data

• Hazardous Substances Data: 82110-13-2(Hazardous Substances Data)

Usage

General Description

(2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol is a chemical compound with the molecular formula C6H12O2. It is a cyclic hemiacetal that belongs to the class of pyran compounds. (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol is chiral, with two stereocenters, and the (2S,4S) configuration indicates that the substituents at these stereocenters are oriented in a specific way. It is commonly used in organic synthesis as a building block for the preparation of more complex molecules. It also has potential applications in the pharmaceutical and fragrance industries due to its ability to impart specific olfactory characteristics. Additionally, (2S,4S)-2-Methyl-tetrahydro-2H-pyran-4-ol has been studied for its potential biological activities, including its antimicrobial and antifungal properties.

Upstream product

• 1193-20-0 2-methyltetrahydro-4H-pyran-4-one 
• 33747-08-9 cis-2-methyltetrahydro-2H-pyran-4-ol 
• 627-27-0 homoalylic alcohol 
• 75-07-0 acetaldehyde 
• 123-20-6 vinyl n-butyrate 

Downstream Products

• 82110-22-3 (2R)-2-methyltetrahydro-4H-pyran-4-one 
• 1193-20-0 2-methyltetrahydro-4H-pyran-4-one 
• 33747-08-9 (2R,4R)-2-methyltetrahydro-2H-pyran-4-ol 
• 82110-21-2 (S)-2-methyl-3,4,5,6-tetrahydro-2H-pyran-4-one 
• 146502-48-9 (2R,4S)-4-(3-Benzyloxy-5-fluoro-phenyl)-2-methyl-tetrahydro-pyran-4-ol 
• 146565-09-5 (2R,4R)-4-(3-Benzyloxy-5-fluoro-phenyl)-2-methyl-tetrahydro-pyran-4-ol 
• 146608-99-3 (2R,4S)-4-(3-Benzyloxy-5-fluoro-phenyl)-4-methoxy-2-methyl-tetrahydro-pyran 
• 146565-12-0 (2R,4R)-4-(3-Benzyloxy-5-fluoro-phenyl)-4-methoxy-2-methyl-tetrahydro-pyran 
• 146565-10-8 (2S,4S)-4-(3-benzyloxy-5-fluorophenyl)-4-hydroxy-2-methyltetrahydropyran 
• 146565-11-9 (2S,4R)-4-(3-Benzyloxy-5-fluoro-phenyl)-2-methyl-tetrahydro-pyran-4-ol 
• 146565-13-1 (2S,4S)-4-<3-(benzyloxy)-5-fluorophenyl>-4-methoxy-2-methyl-3,4,5,6-tetrahydro-2H-pyran 
• 133813-44-2 (2S,4R)-4-<3-(benzyloxy)-5-fluorophenyl>-4-methoxy-2-methyl-3,4,5,6-tetrahydro-2H-pyran 
• 1306729-73-6 MeI 
• 1307304-60-4 ((S)-2-(methoxycarbonylamino)-2-((2S,4R)-2-methyltetrahydro-2H-pyran-4-yl)acetic acid) 

Relevant articles and documents

CYCLIC SUBSTITUTED IMIDAZO[4,5-C]QUINOLINE DERIVATIVES

The present invention provides novel cyclic substituted imidazo[4,5- c]quinoline derivatives of Formula (I), and the pharmaceutically acceptable salts thereof, wherein R1, R2, R4, R5, R6, X and Z are as defined in the specification. The invention is also directed to pharmaceutical compositions comprising the compounds of Formula I and to use of the compounds in the treatment of diseases associated with LRRK2, such as neurodegenerative diseases including Parkinson's disease or Alzheimer's disease, cancer, Crohn's disease or leprosy.

Utilizing on- and off-line monitoring tools to follow a kinetic resolution step during flow synthesis

In situ reaction monitoring tools offer the ability to track the progress of a synthetic reaction in real time to facilitate reaction optimization and provide kinetic/mechanistic insight. Herein, we report the utilization of flow NMR, flow IR, and other off-line spectroscopy tools to monitor the progress of a flow chemistry reaction. The on-line and off-line tools were selected to facilitate the stereoselective kinetic resolution of a key racemic monomer, which lacked a chromophore, making conventional reaction monitoring difficult. Copyright

4-Methoxy-2-methyltetrahydropyrans: Chiral Leukotriene Biosynthesis Inhibitors, Related to ICI D2138, Which Display Enantioselectivity

-