24237-01-2 Usage
Uses
Used in Fragrance Industry:
2-butyl-3,6-dihydro-4,6-dimethyl-2H-pyran is used as a fragrance ingredient in cosmetics, perfumes, and other personal care products due to its sweet, fruity scent. It contributes to the creation of various olfactory profiles in these products, enhancing their appeal to consumers.
Used in Flavor Industry:
In the flavor industry, 2-butyl-3,6-dihydro-4,6-dimethyl-2H-pyran is utilized as a flavoring agent. Its distinctive sweet and fruity aroma makes it suitable for use in food products, adding depth and complexity to the taste profiles of various consumables.
Safety Considerations:
While 2-butyl-3,6-dihydro-4,6-dimethyl-2H-pyran is not considered toxic and is generally regarded as safe for use in the concentrations typically found in consumer products, it is important to note that it may cause irritation to the skin, eyes, and respiratory system in high concentrations. Therefore, appropriate precautions should be taken when handling this substance to minimize potential adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 24237-01-2 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 24237-01:
(7*2)+(6*4)+(5*2)+(4*3)+(3*7)+(2*0)+(1*1)=82
82 % 10 = 2
So 24237-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-4-5-6-11-8-9(2)7-10(3)12-11/h7,10-11H,4-6,8H2,1-3H3
24237-01-2Relevant 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
