62488-56-6 Usage
Description
2,4-Nonadien-1-ol is an organic compound with a green, vegetable odor and a strong fatty, oily taste reminiscent of green melon, cucumber, and chicken or mutton nuances. It is characterized by its waxy, fatty, and aldehydic nuances when present at a 1% concentration.
Uses
Used in Flavor and Fragrance Industry:
2,4-Nonadien-1-ol is used as a flavoring agent for its strong fatty, oily, green melon, and cucumber-like taste, as well as its chicken and mutton nuances. It is particularly suitable for enhancing the taste of various food products.
2,4-Nonadien-1-ol is also used as a fragrance ingredient for its green, vegetable odor, making it a valuable component in the creation of perfumes and other scented products.
Used in Aromatherapy:
Due to its pleasant and distinctive aroma, 2,4-Nonadien-1-ol can be used in aromatherapy as a means to promote relaxation and a sense of well-being.
Used in the Chemical Industry:
2,4-Nonadien-1-ol's unique chemical properties make it a potential candidate for various chemical applications, such as the synthesis of other compounds or as an intermediate in the production of specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 62488-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,8 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62488-56:
(7*6)+(6*2)+(5*4)+(4*8)+(3*8)+(2*5)+(1*6)=146
146 % 10 = 6
So 62488-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c1-2-3-4-5-6-7-8-9-10/h5-8,10H,2-4,9H2,1H3
62488-56-6Relevant articles and documents
Synthesis of α,β-Unsaturated Aldehydes through Palladium Catalyzed Regioselective Hydrogen Migration
Minami, Tatsuya,Hanaoka, Miyoji
, p. 9425 - 9428 (2007/10/02)
Treatment of cyclic carbonate of 3-alkene-1,2-diols or 4-methylcarbonate of 2-alkene-1,4-diols with a catalytic amount of Pd(PPh3)4 in aqueous THF or AcOH gave α,β-unsaturated aldehydes in good yields.The reaction can be interpreted by the regioselective 1,4-hyrogen migration of ?-allylpalladium intermediate.
