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2,4-Cycloheptadien-1-one, 3,6,6-trimethyl- is an organic compound with the molecular formula C10H16O. It is a cyclic ketone, characterized by the presence of a carbonyl group (C=O) and a seven-membered ring structure. The compound has three methyl groups (CH3) attached to the carbon atoms at positions 3, 6, and 6, which contribute to its unique chemical properties. 2,4-Cycloheptadien-1-one, 3,6,6-trimethyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of fragrances and flavorings. Due to its complex structure and functional groups, it is essential to handle this chemical with care, following proper safety protocols to minimize potential health and environmental risks.

2767-18-2

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2767-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2767-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2767-18:
(6*2)+(5*7)+(4*6)+(3*7)+(2*1)+(1*8)=102
102 % 10 = 2
So 2767-18-2 is a valid CAS Registry Number.

2767-18-2Downstream Products

2767-18-2Relevant academic research and scientific papers

Method of preparing 3-isopropyl-5-cresol and carvacrol with 3-carene

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Paragraph 0075; 0076; 0077, (2019/02/04)

The invention discloses a method of preparing 3-isopropyl-5-cresol and carvacrol with 3-carene. The method comprises the following steps that 3-carene is reacted with oxygen at a room temperature to produce a product I under the catalysis of CrO3-Al2O3, wherein the product I is prepared from the main components including 5-carone, 2-carone and 4-carone with the selectivity ratio being about 10.8 to 3.5 to 1.0; the product I is distilled to recover 3-carene, wherein the recovery rate is larger than 80 percent, and the recovery purity is larger than 94 percent; the residual components are converted to a product II at 230 DEG C under catalysis of a 13X type molecular sieve, and reduced pressure distillation is performed on the product II to obtain a mixed phenol product with the purity largerthan 96 percent, wherein the product II is prepared from the main components including 3-isopropyl-5-cresol and carvacrol, the raw material conversion rate is 100 percent, the total selectivity of phenolic products can reach 98 percent, and the selectivity ratio of the two phenolic products is about 2.2 to 1.0; and column chromatography isolation is performed on the product II to obtain 3-isopropyl-5-cresol and carvacrol with the purities larger than 97 percent respectively.

Reactions of some terpenes and their derivatives with acylating agents in the presence of aluminosilicate catalysts

Volcho,Tatarova,Suslov,Korchagina,Salakhutdinov,Barkhash

, p. 1418 - 1429 (2007/10/03)

Reactions of camphene, α-fenchene, limonene, caryophyllene, α- and β-pinenes, verbenol, walterol, and verbenone with acylating agents in the presence of clay K-10 and wide-porous β-zeolite were studied. Presumable schemes and rules of the occurring proces

INTRODUCTION OF OXYGENATED FUNCTIONAL GROUPS INTO 3-CARENE AND 2-PINENE BY CULTURED CELLS

Hirata, Toshifumi,Ikeda, Yoshihiro,Izumi, Shunsuke,Shimoda, Kei,Hamada, Hiroki,Kawamura, Toshinari

, p. 401 - 404 (2007/10/02)

The biotransformation of the monoterpene hydrocarbons 3-carene and 2-pinene by cell suspension cultures of Nicotiana tabacum and Catharanthus roseus was investigated.The cultures have the ability to regio- and enantioselectively introduce the oxygenated functional groups into the C=C double bond and the allylic positions of the substrates. - Key words: Nicotiana tabacum; Solanaceae; Catharanthus roseus; Apocyanaceae; cultured cells; biotransformation; epoxidation; hydroxylation; carene; pinene.

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