基本情報
- 標準SMILES
O=C1CCc2ccccc2C1- InChIKey
KCKZIWSINLBROE-UHFFFAOYSA-N- 分子式
- C10H10O
- 平均分子量
- 146.19 g/mol
- 単同位体質量
- 146.07316494
名称と識別子
- 優先名称
- 2-Tetralone
- IUPAC
- 3,4-dihydro-1H-naphthalen-2-one
- 現地名
- β-テトラロン
- 英語名
- beta-Tetralone
- 分子式
- C10H10O
- 分子量
- 146.19
名称と別名
名称をさらに表示
データベース識別子
- CAS
530-93-8- PubChem CID
- 68266
- DTXSID
DTXSID0060193- ChEMBL
CHEMBL191664- UNII
- K46ZZ833BH
- EC Number
- 208-498-3
- Nikkaji
- J6.975B
物性
構造計算による物性
- XLogP
- 1.6
- 極性表面積
- 17.1 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 1
- 回転可能結合数
- 0
- 重原子数
- 11
- 形式電荷
- 0
- 複雑度
- 162
実験および物理化学的性質
物理化学的性質
- 融点
- 18 °C · 18 °C(lit.)
- 沸点
- 131 °C11 · 131 °C11 mm Hg(lit.)
- 比重(密度)
- 1.106 g/mL · 1.106 g/mL at 25 °C(lit.)
- 屈折率
- 20 · n20/D 1.560(lit.)
- 闪点
- 230 °F · >230 °F
- 貯蔵温度
- 2 · 2-8°C
- 溶解性
- クロロホルム(微量)、酢酸エチル(微量)
- 外見
- 液体または低融点固体
- 色
- 澄んだ薄黄色
- 水溶解度
- 不溶性
- BRN
- 509386 · 509386
- InChI
- 1S/C10H10O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-4H,5-7H2
- InChIKey
- KCKZIWSINLBROE-UHFFFAOYSA-N
- SMILES
- O=C1CCc2ccccc2C1
- CAS データベース
- 530 · 530-93-8(CAS DataBase Reference)
- NISTの化学物質情報
- 2 · 2(1H)-Naphthalenone, 3,4-dihydro-(530-93-8)
- EPAの化学物質情報
- 2 · 2-Tetralone (530-93-8)
化学的性質
化学的特性Liquid colorless to yellow
安全と法規制
GHS分類
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 40 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
安全データ
- F
- 10
- wgk
- 3
- tsca
- TSCA listed
- hs_code
- 29143900
- risk_code
- 36/37/38-20/21/22
- 消防法
- 危-4-3-III
- hazard_code
- Xi,Xn
- safety_code
- 26-36
- ストレージクラス
- 10 - Combustible liquids
化学と産業
用途と製造
応用分野
使用β-Tetralone is the 2-keto derivative of Tetralin. β-Tetralone was initially reported to be a metabolite of Tetralin but was later found to be just an artifact in the metabolism process. β-Tetralone is known to be biological marker in fossil fuels.
調製方法
純化方法If reasonably pure, then fractionate it through an efficient column. Otherwise purify it via the bisulfite adduct. To a solution of NaHSO3 (32.5g, 0.31mol) in H2O (57mL) is added 95% EtOH (18mL) and set aside overnight. Any bisulfite-sulfate that separated is removed by filtration, and the filtrate is added to the tetralone (14.6g, 0.1mol) and shaken vigorously. The adduct separates in a few minutes as a white precipitate and is kept on ice for ~3.5hours with occasional shaking. The precipitate is collected, washed with 95% EtOH (13mL), then with Et2O (4 x 15mL, by stirring the suspension in the solvent, filtering and repeating the process). The colourless product is dried in air and stored in air tight containers in which it is stable for extended periods (yield is ~17g). This bisulfite (5g) is suspended in H2O (25mL), and Na2CO3.H2O (7.5g) is added (pH of solution is ~10). The mixture is then extracted with Et2O (5 x 10mL, i.e. until the aqueous phase does not test for tetralone — see below). Wash the combined extracts with 10% aqueous HCl (10mL), H2O (10mL, i.e. until the washings are neutral), dry (MgSO4), filter, evaporate and distil the residual oil using a Claisen flask under reduced pressure and in a N2 atmosphere. The pure tetralone is a colourless liquid b 70-71o/0.25mm (see also above). The yield is ~2g. Tetralone test: Dissolve a few drops of the tetralone solution (ethereal or aqueous) in 95% EtOH in a test tube and add 10 drops of 25% NaOH down the side of the tube. A deep blue colour develops at the interface with air. [Soffer et al. Org Synth Coll Vol IV 903 1963, Cornforth et al. J Chem Soc 689 1942, UV: Soffer et al. J Am Chem Soc 1556 1952.] The phenylhydrazone has m 108o [Crawley & Robinson J Chem Soc 2001 1938]. [Beilstein 7 H 370, 7 II 295, 7 III 1422, 7 IV 1018.]
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下流製品
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