基本情報
- 標準SMILES
C=Cc1ccc(Br)cc1- InChIKey
WGGLDBIZIQMEGH-UHFFFAOYSA-N- 分子式
- C8H7Br
- 平均分子量
- 183.04 g/mol
- 単同位体質量
- 181.97311232
概要
structure in first source
名称と識別子
- 優先名称
- 4-Bromostyrene
- IUPAC
- 1-bromo-4-ethenylbenzene
- 現地名
- 4-ブロモスチレン
- 英語名
- 4-Bromostyrene
- 分子式
- C8H7Br
- 分子量
- 183.05
名称と別名
名称をさらに表示
データベース識別子
- CAS
2039-82-9- PubChem CID
- 16263
- DTXSID
DTXSID40174330- UNII
- TVK4S80XLU
- EC Number
- 218-022-6
- Nikkaji
- J7.855G
物性
構造計算による物性
- XLogP
- 3.4
- 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
- 1
- 重原子数
- 9
- 形式電荷
- 0
- 複雑度
- 90.7
実験および物理化学的性質
物理化学的性質
- 融点
- 4.5 °C · 4.5 °C
- 沸点
- 89 °C16 · 89 °C16 mm Hg(lit.)
- 比重(密度)
- 1.4 g/mL · 1.40 g/mL at 20 °C
- 屈折率
- 20 · n20/D 1.594(lit.)
- 闪点
- 168 °F · 168 °F
- 貯蔵温度
- -20 °C · -20°C
- 溶解性
- エタノール、エーテル、ベンゼンと混和します。
- 外見
- 液体
- 色
- 薄緑がかった黄色
- BRN
- 1634204 · 1634204
- InChI
- InChI=1S/C8H7Br/c1-2-7-3-5-8(9)6-4-7/h2-6H,1H2
- InChIKey
- WGGLDBIZIQMEGH-UHFFFAOYSA-N
- SMILES
- C1(Br)=CC=C(C=C)C=C1
- CAS データベース
- 2039 · 2039-82-9(CAS DataBase Reference)
- NISTの化学物質情報
- 4 · 4-BrC6H4CH=CH2(2039-82-9)
化学的性質
化学的特性clear slightly yellow to yellow liquid
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 49 reports by companies from 7 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
- 8
- wgk
- 3
- hs_code
- 29036990
- risk_code
- 36/38-36/37/38
- 消防法
- 危-4-3-III
- hazard_code
- Xi
- hazard_note
- Irritant/Keep Cold
- safety_code
- 26-36-37/39
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2
- ストレージクラス
- 10 - Combustible liquids
化学と産業
応用分野
使用4-Bromostyrene is widely utilized in the synthesis of nitroolefins by alkene cross-metathesis. It plays an important role in the Heck reaction to the synthesis of poly(1,4-phenylenevinylene). It is employed in the structure activity relationships (SAR) study of the chemical and biochemical properties of the vinyl group of styrene. It is also used to investigate the photochemical growth of Br-terminated self-assembled monolayers. It is also involved in the synthesis of silsesquioxanes.
一般的な説明4-Bromostyrene is a para-halogenated styrene derivative. The proton spectra of 4-bromostyrene exhibits dipolar couplings consistent with planar ground state structures, only if the torsional motion of lowest frequency occurs at about 80cm-1. It undergoes Heck reaction with 2-bromo-6-methoxynaphthalene in the presence of sodium acetate and Hermann′s catalyst in N,N-dimethylacetamide to afford diarylethene.
調製方法
純化方法It polymerises above 75o in the presence of benzoyl peroxide. To purify, if it has not gone to a solid resin, dissolve it in Et2O, dry (MgSO4) and add ca 0.1g of 4-tertbutylcatechol (polymerisation inhibitor) per 100g of bromostyrene. Filter, evaporate this under reduced pressure (use as high a vacuum as possible) and distil the residue. Store it in dark bottles in the presence of the inhibitor (at above concentration). [Overberger & Saunders Org Synth Coll Vol III 204 1955, Beilstein 5 IV 1349.]
上流・下流製品情報
下流製品
サプライヤー50 社
関連反応
関連ノート
読み込み中…