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2-butoxy-3,4-dihydro-4-phenyl-2H-pyran is a colorless liquid chemical compound with the molecular formula C14H20O2. It is commonly used in various industries due to its versatile properties.

324-00-5

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324-00-5 Usage

Uses

Used in Fragrance Industry:
2-butoxy-3,4-dihydro-4-phenyl-2H-pyran is used as a fragrance ingredient for its aromatic properties, adding pleasant scents to perfumes and personal care products.
Used in Food Industry:
In the food industry, 2-butoxy-3,4-dihydro-4-phenyl-2H-pyran is used as a flavoring agent to enhance the taste and aroma of food products.
Used in Plastics Industry:
2-butoxy-3,4-dihydro-4-phenyl-2H-pyran is utilized in the production of plasticizers, which are added to plastics to improve their flexibility and durability.
Used in Pesticide Production:
This chemical compound is also used in the manufacturing of pesticides, contributing to the effectiveness of these agricultural products.
Used as a Solvent in Industrial Applications:
2-butoxy-3,4-dihydro-4-phenyl-2H-pyran serves as a solvent in various industrial processes, aiding in the dissolution and mixing of substances.
Safety Note:
While 2-butoxy-3,4-dihydro-4-phenyl-2H-pyran is not known to be highly toxic or harmful to humans, it may cause irritation to the eyes, skin, and respiratory tract upon direct contact or inhalation. Therefore, it should be handled with care to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 324-00-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 324-00:
(5*3)+(4*2)+(3*4)+(2*0)+(1*0)=35
35 % 10 = 5
So 324-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O2/c1-2-3-10-16-15-12-14(9-11-17-15)13-7-5-4-6-8-13/h4-9,11,14-15H,2-3,10,12H2,1H3

324-00-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butoxy-4-phenyl-3,4-dihydro-2H-pyran

1.2 Other means of identification

Product number -
Other names 2-Butoxy-3,4-dihydro-4-phenyl-2H-pyran

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:324-00-5 SDS

324-00-5Relevant academic research and scientific papers

6-O-acyl ketolide antibacterials

-

, (2008/06/13)

6-O-Acyl ketolide antibacterials of the formula: wherein R1, R2, R3, R4, W, X, X′, Y, and Y′ are as described herein and in which the substituents have the meaning indicated in the description. These compounds are useful as antibacterial agents.

6-O-carbamoyl ketolide antibacterials

-

, (2008/06/13)

6-O-Carbamoyl ketolide antibacterials of the formula: wherein R1, R2, R3, R4, R5, R6, X, X′, Y, and Y′ are as described herein and in which the substituents have the meaning indicated in the description. These compounds are useful as antibacterial agents.

6-0-carbamoyl ketolide antibacterials

-

, (2008/06/13)

6-O-Carbamoyl ketolide antibacterials of the formula: wherein R1, R2, R3, R4, R5, R6, X, X′, Y, and Y′ are as described herein and in which the substituents have the meaning indicated in the description. These compounds are useful as antibacterial agents.

Experimental studies of the anomeric effect. Part III. Rotameric preferences about the exo-cyclic c2-x bond in equatorial and axial 2-methoxy-and 2-methylamino-tetrahydropyrans

Booth, Harold,Dixon, J. Mark,Khedhair, Khedhair A.,Readshaw, Simon A.

, p. 1625 - 1652 (2007/10/02)

Values of3 J(CC), 3J(CH), 4J(CH) and 3J(HH), supported by n.O.enhancements, in nmr spectra of 2-methoxy- and 2-methyl-amino-tetrahydropyrans, point to a very strong preference for rotamers in which an exo-cyclic heteroatom lone pair is antiperiplanar to the endo-cyclic C2-O bond ("endo-anomeric effect").

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