183551-55-5

Basic information

• Product Name: (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE
• Synonyms: (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE
• CAS NO: 183551-55-5
• Molecular Formula: C₁₀H₂₁NO₂
• Molecular Weight: 187.28
• Mol File: 183551-55-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 95℃
• Appearance: /
• CAS DataBase Reference: (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE(183551-55-5)
• EPA Substance Registry System: (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE(183551-55-5)

Safety Data

• Hazardous Substances Data: 183551-55-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE is used as a building block for the synthesis of various pharmaceuticals, leveraging its unique structural features and reactivity to create complex molecules with specific stereochemistry.
Used in Organic Synthesis:
In the field of organic synthesis, (R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE is used as a reagent, taking advantage of its structural characteristics and reactivity to facilitate the creation of complex molecules with desired stereochemistry.
Used in Medicinal Chemistry Research:
(R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE is utilized in medicinal chemistry research for its potential applications in the development of new drugs and therapies, given its biological activity and the possibility of incorporating it into novel pharmaceutical compounds.
Used in Chemical Research:
(R)-3-METHYL-4-TETRAHYDROPYRANYLOXYBUTYLAMINE is also used in chemical research to explore its properties, reactivity, and potential applications in creating new molecules and materials with specific characteristics.

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 44565-27-7 (R)-4-amino-2-methyl-1-butanol 
• 67000-01-5 methyltertbutyl ether 

Downstream Products

• 217099-10-0 7-[(R)-3-Methyl-4-(tetrahydro-pyran-2-yloxy)-butyl]-8-oxo-5-p-tolyl-7,8-dihydro-[1,7]naphthyridine-6-carboxylic acid 3,5-bis-trifluoromethyl-benzylamide 
• 183549-95-3 (aR,9R)-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,11-tetrahydro-9-methyl-5-(4-methylphenyl)-7H-[1,4]diazocino[2,1-g][1,7]naphthyridine-6,13-dione 
• 183549-95-3 (aS,9R)-7-[3,5-bis(trifluoromethyl)benzyl]-8,9,10,11-tetrahydro-9-methyl-5-(4-methylphenyl)-7H-[1,4]diazocino[2,1-g][1,7]naphthyridine-6,13-dione 
• 183551-02-2 (R)-N-[3,5-bis(trifluoromethyl)benzyl]-7,8-dihydro-7-(4-hydroxy-3-methylbutyl)-5-(4-methylphenyl)-8-oxo-1,7-naphthyridine-6-carboxamide 

Relevant articles and documents

PROCESS FOR PREPARATION OF TETRAHYDROPYRANYLOXYAMINES

Tetrahydropyranyloxyamines are extremely useful as intermediates in the production of pharmaceuticals and agricultural chemicals, and as raw materials, additives or precursors in the production of perfumes, resins and adhesives. The present invention provides a process for producing a tetrahydropyranyloxyamine from an aminoalcohol which is both simple and produces a high yield. According to the present invention, an aminoalcohol represented by a general formula (1) shown below is reacted with an acid, the obtained aminoalcohol salt is reacted with 3,4-dihydro-2H-pyran, and the obtained tetrahydropyranyloxyamine salt is subsequently reacted with an alkali to form a tetrahydropyranyloxyamine represented by the general formula (2) shown below.H2N―X―OH (wherein in said formula (1) and said formula (2), X represents a methylene group, an ethylene group or a straight chain polymethylene group having 3 to 20 carbon atoms)