67401-26-7 Usage
General Description
(E)-3-(2-butenyl)-2,4,4-trimethylcyclohex-2-en-1-one, also known as rhodinol, is a fragrance compound commonly found in essential oils and used in perfumery. It is a cyclic ketone with a floral, woody, and slightly fruity odor. Rhodinol is found in a variety of natural sources such as roses, geraniums, and tobacco. It is widely utilized as a fragrance ingredient in various products such as perfumes, scented candles, and air fresheners due to its pleasant and long-lasting scent. Additionally, (E)-3-(2-butenyl)-2,4,4-trimethylcyclohex-2-en-1-one is also used in the formulation of personal care and household products.
Check Digit Verification of cas no
The CAS Registry Mumber 67401-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,0 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67401-26:
(7*6)+(6*7)+(5*4)+(4*0)+(3*1)+(2*2)+(1*6)=117
117 % 10 = 7
So 67401-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O/c1-5-6-7-11-10(2)12(14)8-9-13(11,3)4/h5-6H,7-9H2,1-4H3/b6-5+
67401-26-7Relevant articles and documents
New methods for the preparation of theaspiranes, megastigmane-5,7,9-trien-4-one and megastigmane-5,8-dien-4-one from γ-pyronene
Boulin,Arreguy-San Miguel,Delmond
, p. 3927 - 3932 (2007/10/03)
γ-Pyronene, a terpenic synthon easily available from myrcene, an industrial raw material, is used as an intermediate in the synthesis of theaspiranes and various megastigmane derivatives. These compounds are useful in the preparation of perfumes and aromas. (C) 2000 Elsevier Science Ltd.
Isolation and synthesis of 3-(2-butenyl)-2,4,4-trimethyl-2-cyclohexen-1-one. Regiospecific oxidation of 1-(2-butenyl)-2,6,6-trimethylcyclohexene
Weerdt, Anton J. A. van der,Apeldoorn, Willem,Boelens, Mans,Koenst, Wil M. B.,Heide, Roel ter
, p. 447 - 449 (2007/10/02)
(E)- and (Z)-3-(2-butenyl)-2,4,4-trimethyl-2-cyclohexen-1-one 1 and 2 have been isolated from an absolue of Osmanthus Fragrance Lour, and a fusel oil concentrate.Structural proof for these compounds has been obtained via their synthesis from β-ionone.The key step in this synthesis is the regio-specific oxidation of 1-(2-butenyl)-2,6,6-trimethylcyclohexene.