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2-Butyltetrahydro-6-methyl-4-methylene-2H-pyran is a chemical compound belonging to the tetrahydropyran class, specifically as a tetrahydropyran derivative. It has the molecular formula C11H18O and is characterized by its colorless or pale yellow liquid appearance, strong odor, and solubility in organic solvents.

24237-02-3

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24237-02-3 Usage

Uses

Used in Flavor and Fragrance Industry:
2-Butyltetrahydro-6-methyl-4-methylene-2H-pyran is used as a flavoring agent and fragrance component for its distinctive scent and taste, contributing to the creation of various consumer products.
Used as a Chemical Intermediate:
In the chemical industry, 2-butyltetrahydro-6-methyl-4-methylene-2H-pyran serves as a valuable intermediate in the synthesis of other compounds, facilitating the production of a range of chemical products.
Safety Precautions:
It is crucial to handle 2-butyltetrahydro-6-methyl-4-methylene-2H-pyran with care due to its potential harmful effects if inhaled, swallowed, or absorbed through the skin. Proper safety measures should be taken during its use and storage to minimize health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 24237-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,3 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24237-02:
(7*2)+(6*4)+(5*2)+(4*3)+(3*7)+(2*0)+(1*2)=83
83 % 10 = 3
So 24237-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-4-5-6-11-8-9(2)7-10(3)12-11/h10-11H,2,4-8H2,1,3H3

24237-02-3Upstream product

24237-02-3Downstream Products

24237-02-3Relevant academic research and scientific papers

Enzymatic approach to enantiomerically pure 5-alken-2,4-diols and 4-hydroxy-5-alken-2-ones: Application to the synthesis of chiral synthons

Abate, Agnese,Brenna, Elisabetta,Costantini, Alessia,Fuganti, Claudio,Gatti, Francesco G.,Malpezzi, Luciana,Serra, Stefano

, p. 5228 - 5240 (2007/10/03)

Enantiomerically pure 1,3-diols 1-3 were obtained by a chemoenzymatic approach (lipase PS from Burkholderia cepacia). These diols were converted into useful chiral synthons, which could be considered homologues of glyceraldehyde and glyceric acid acetonid

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