9,10-ジブロモアントラセン

9,10-Dibromoanthracene

HCID 68226CAS 523-27-3

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

9,10-Dibromoanthracene523-27-3Anthracene, 9,10-dibromo-DTXSID5049312UNII-61CP7C5Y8261CP7C5Y82NSC 6263NSC-6263EINECS 208-342-4DTXCID00292689,10-DIBROMOANTHRACENE [MI]RefChem:107475
名称をさらに表示
9,10-ジブロモアントラセンms-ジブロモアントラセン9,10ジブロモアントラセン9,10‐ジブロモアントラセン9,10-Dibromoanthracene99%9,10-anthracenems-Dibromoanthracene9, 10-Dibromoanthrac10-Dibromoanthracene9,I O-Dibromanthracen9,1-Dibromoanthracene9,1O-dibromoanthracene9,10-DIRBOMOANTHRACENE
Anthracene, 9,10dibromo52f3-27-3208-342-4BRUOAURMAFDGLP-UHFFFAOYSA-NInChI=1/C14H8Br2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-89,10-Dibromo-anthraceneMFCD00001244NSC 6263;

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

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
化学的性質 · 1 件

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

化学と産業

応用分野 · 3 件

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 · 2 件

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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関連反応

32 件

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