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化驗
98%
折射率
n20/D 1.494 (lit.)
bp
199-200 °C (lit.)
密度
0.971 g/mL at 25 °C (lit.)
SMILES 字串
CC1=CC(=O)CCC1
InChI
1S/C7H10O/c1-6-3-2-4-7(8)5-6/h5H,2-4H2,1H3
InChI 密鑰
IITQJMYAYSNIMI-UHFFFAOYSA-N
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應用
3-Methyl-2-cyclohexenone is an insect sex pheromone of the Douglas-fir beetle. It can be used as a starting material:
- In the total synthesis of (−)-ar-tenuifolene, a naturally occurring aromatic sesquiterpene.
- To synthesize an organic building block 2-trimethylsilyl-3-methyl-cyclohexenone.
- In the total synthesis of natural diterpenoids (+)-taiwaniaquinone H and (+)-dichroanone.
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
154.4 °F - closed cup
閃點（°C）
68 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Catalytic asymmetric formal total synthesis of (+)-dichroanone and (+)-taiwaniaquinone H
Li L-Q, et al.
Tetrahedron Letters, 55(43), 5960-5962 (2014)
Cyclic α-Acylvinyl Anionic Synthons: A Novel Synthesis of 2-Trimethylsilyl-3-methyl-cyclohexenone by the Wurtz-Fittig Coupling Reaction
Jyothi D and HariPrasad S
Synthetic Communications, 39(5), 875-879 (2009)
Catalytic enantioselective total synthesis of (−)-ar-Tenuifolene
Shaw K, et al.
Tetrahedron Letters, 61(20), 151850-151850 (2020)
Chemical transformation of 1, 8-cineole: synthesis of seudenone, an insect pheromone
Silvestre AJD, et al.
Industrial Crops and Products, 12(1), 53-56 (2000)
Aldrichimica Acta, 16, 41-41 (1983)
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