10160-25-5

Basic information

• Product Name: 2-(7-Bromoheptyloxy)tetrahydro-2H-pyran
• Synonyms: 2-(7-Bromoheptyloxy)tetrahydro-2H-pyran;2-[(7-Bromoheptyl)oxy]tetrahydro-2H-pyran
• CAS NO: 10160-25-5
• Molecular Formula: C₁₂H₂₃BrO₂
• Molecular Weight: 0
• Mol File: 10160-25-5.mol
• Article Data: 34

Chemical Properties

• Appearance: /
• Solubility: DCM, EtOAc, Hexane
• CAS DataBase Reference: 2-(7-Bromoheptyloxy)tetrahydro-2H-pyran(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(7-Bromoheptyloxy)tetrahydro-2H-pyran(10160-25-5)
• EPA Substance Registry System: 2-(7-Bromoheptyloxy)tetrahydro-2H-pyran(10160-25-5)

Safety Data

• Hazardous Substances Data: 10160-25-5(Hazardous Substances Data)

Usage

Uses

2-(7-Bromoheptyloxy)tetrahydropyran is an intermediate in the synthesis of (8E)-Dodecen-1-ol (D525705) which is used in the study of the photochemical transformations of biologically active mono- and diene derivatives of pheromones.

Upstream product

• 74473-94-2 hydrangenoside B pentaacetate 
• 132336-04-0 2-(heptyloxy)tetrahydro-2H-pyran 
• 110-87-2 3,4-dihydro-2H-pyran 
• 10160-24-4 7-bromoheptyl alcohol 
• 111-70-6 n-heptan1ol 
• 629-30-1 1,7-heptandiol 

Downstream Products

• 4273-95-4 (Z)-11-octadecenal 
• 56683-54-6 (Z)-11-hexadecen-1-ol 
• 62972-93-4 (Z)-octadec-11-en-1-ol 
• 34010-21-4 (Z)-11-hexadecen-1-yl acetate 
• 1448019-30-4 2-[(R)-16-(benzyloxy)-14-methylhexadec-8-ynyloxy]tetrahydro-2H-pyran 
• 66007-17-8 (S)-14-Methyl-(Z)-8-hexadecenal 
• 66007-19-0 (S,E)-(+)-14-methyl-8-hexadecenal (trogodermal) 
• 1402547-75-4 13-(tert-butyldiphenylsilyloxy)tridec-8(Z)-enoic acid 
• 622842-70-0 13-(tert-butyldiphenylsilyloxy)tridec-8(Z)-en-1-ol 
• 240427-79-6 1-(tert-butyldiphenylsilyloxy)-tridec-5-yn-13-ol 
• 1402547-48-1 13-(3-N-pentylureido)-N-(phenylsulfonyl)tridec-8(Z)-enamide 
• 57586-92-2 14-tetrahydropyranyloxy-2(E)-tetradecene 
• 17257-41-9 methyl vaccenate 
• 18545-05-6 octadec-8-ynoic acid methyl ester 

Relevant articles and documents

Synthesis and bioactivity of linear oligomers related to polymeric alkylpyridinium metabolites from the Mediterranean sponge Reniera sarai

Dimers and tetramers of linear 3-alkylpyridinium salts have been synthesized by an efficient synthetic pathway, which is also applicable to the preparation of higher oligomers. Mono-, di- and tetrameric compounds have been tested for antibacterial and hem

PYRIDINE COMPOUND SUBSTITUTED WITH AZOLE

The present invention provides a compound represented by formula [I] shown below or a pharmaceutically acceptable salt thereof that has an inhibitory effect on 20-HETE producing enzyme. (in formula [I] above, the structure represented by formula [II] below: represents any of the structures represented by formula group [III] below: R1, R2, R3, and R4 independently represent a hydrogen atom, a fluorine atom, methyl, or the like, R5 represents any of the structures represented by formula group [IV]:

Method for synthesizing cis-7-tetradecenol acetate which is main component of sex pheromone of holcocerus vicarius walker

The invention discloses a method for synthesizing cis-7- tetradecenol acetate which is a main component of sex pheromone of holcocerus vicarius walker. The method includes (1), preparing (7-bromo-heptyl-1-)-2-tetrahydropyran ether; (2), preparing (7-bromo