基本情報
- 標準SMILES
Brc1c2ccccc2c(Br)c2ccccc12- InChIKey
BRUOAURMAFDGLP-UHFFFAOYSA-N- 分子式
- C14H8Br2
- 平均分子量
- 336.02 g/mol
- 単同位体質量
- 333.89928
名称と識別子
- 優先名称
- 9,10-Dibromoanthracene
- IUPAC
- 9,10-dibromoanthracene
- 現地名
- 9,10-ジブロモアントラセン
- 英語名
- 9,10-Dibromoanthracene
- 分子式
- C14H8Br2
- 分子量
- 336.02
名称と別名
名称をさらに表示
データベース識別子
- CAS
523-27-3- PubChem CID
- 68226
- DTXSID
DTXSID5049312- ChEMBL
CHEMBL3183379- UNII
- 61CP7C5Y82
- EC Number
- 208-342-4
- Nikkaji
- J6.630C
物性
構造計算による物性
- XLogP
- 5.8
- 極性表面積
- 0 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 0
- 回転可能結合数
- 0
- 重原子数
- 16
- 形式電荷
- 0
- 複雑度
- 203
物理化学的性質
- 融点
- 223 · 223-224 °C (lit.)
- 沸点
- 342.21 °C · 342.21°C (rough estimate)
- 比重(密度)
- 1.7167 · 1.7167 (estimate)
- 屈折率
- 1.63 · 1.6300 (estimate)
- 貯蔵温度
- Sealed in dry,Room Temperature
- 溶解性
- クロロホルム
- 外見
- ふわふわパウダー
- 色
- 黄色から黄緑色
- 水溶解度
- 水に溶ける。
- Merck
- 14 · 14,3018
- BRN
- 1912109 · 1912109
- InChI
- 1S/C14H8Br2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
- InChIKey
- BRUOAURMAFDGLP-UHFFFAOYSA-N
- SMILES
- Brc1c2ccccc2c(Br)c3ccccc13
- CAS データベース
- 523 · 523-27-3(CAS DataBase Reference)
- NISTの化学物質情報
- 9 · Anthracene, 9,10-dibromo-(523-27-3)
- EPAの化学物質情報
- 9 · Anthracene, 9,10-dibromo- (523-27-3)
化学的性質
化学的特性Yellow to yellow-green fluffy powder. Melting point 226°C. It can be sublimated and oxidized to generate anthraquinone. It is soluble in hot benzene and hot toluene, but only slightly soluble in alcohol, ether, and cold benzene. It is insoluble in water.
安全と法規制
安全データ
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 3077
- hs_code
- 29039990
- risk_code
- 36/37/38-50/53
- hazard_code
- Xi,N
- safety_code
- 37/39-26-61-60-36
- hazard_class
- 9
- Hazard Classifications
- Aquatic Acute 1Aquatic Chronic 1
- ストレージクラス
- 11 - Combustible Solids
化学と産業
応用分野
用途有機合成原料。
説明9,10-Dibromoanthracene is an organic chemical compound containing anthracene with two bromine atoms substituted on its central ring. As a symmetrically brominated anthracene derivative, it is bearing functional groups to extend its conjugation further mainly via C-C bond forming i.e. Stille and Suzuki coupling reactions. It is notable in that it was the first single molecule to have a chemical reaction observed by an atomic force microscope and scanning tunneling microscopy. It is a low-molecular-weight organic semiconductor. It can used as an initiator in visible-spectrum solar-light-mediated benzylic C–H oxygenation through solar light or the blue LED activate[1-2].
使用9,10-Dibromoanthracene is a dibrominated polycyclic aromatic hydrocarbon (PAH). 9,10-Dibromoanthracene is often used as an energy acceptor and activator in reactions that produce chemiluminescence.
調製方法
製造方法9,10-Dibromoanthracene is synthesized by the bromination of anthracene. The bromination reaction is carried out at room temperature using carbon tetrachloride as a solvent. Using 80-85% anthracene as raw material, adding bromine to react for half an hour, the yield is 83-88%.
純化方法Recrystallise it from toluene, xylene or CCl4 (yellow needles), and sublime it in a vacuum [Johnston et al. J Am Chem Soc 109 1291 1987]. [Heilbron & Heaton Org Synth Coll Vol I 207 1941, Beilstein 5 H 665.]
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