基本情報
- 標準SMILES
c1nnco1- InChIKey
FKASFBLJDCHBNZ-UHFFFAOYSA-N- 分子式
- C2H2N2O
- 平均分子量
- 70.05 g/mol
- 単同位体質量
- 70.01671268
概要
structure in first source
名称と識別子
- 優先名称
- 1,3,4-Oxadiazole
- IUPAC
- 1,3,4-oxadiazole
- 現地名
- 1,3,4-オキサジアゾール
- 英語名
- 1,3,4-oxadiazole
- 分子式
- C2H2N2O
- 分子量
- 70.05
名称と別名
名称をさらに表示
データベース識別子
- CAS
288-99-3- PubChem CID
- 97428
- DTXSID
DTXSID10182987- UNII
- 20O2F20OUR
- EC Number
- 873-098-3
- Nikkaji
- J327.198F
物性
構造計算による物性
- XLogP
- -0.2
- 極性表面積
- 38.9 Ų
- 水素結合供与体数
- 0
- 水素結合受容体数
- 3
- 回転可能結合数
- 0
- 重原子数
- 5
- 形式電荷
- 0
- 複雑度
- 26.8
実験および物理化学的性質
物理化学的性質
- 沸点
- 121.44 °C · 121.44°C (rough estimate)
- 比重(密度)
- 1.2619 · 1.2619 (rough estimate)
- 屈折率
- 1.43 · 1.4300 (estimate)
- 貯蔵温度
- Refrigerator, Under inert atmosphere
- 溶解性
- クロロホルム(可溶)、メタノール(微量)
- 外見
- 油
- 酸解離定数(Pka)
- -3.82 · -3.82±0.22(Predicted)
- 色
- 無色
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)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
危険有害性情報
安全データ
- 危険有害性情報
- コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード H315
化学と産業
応用分野
説明1,3,4-Oxadiazole is a five-membered, conjugated, planar, stable heteroaromatic, comprised of two adjacent nitrogen atoms at the 3,4-positions with one oxygen atom and two vicinal carbon atoms. Each nitrogen atom in the ring is one carbon apart from the oxygen heteroatom. The 1,3,4-oxadiazole ring is electron deficient due to the presence of two pyridine-like nitrogen atoms in the ring and as a result its chemical properties are unlike those of furan as evidenced from the downfield chemical shift of C2(5)H at δ 8.73 ppm (CDCl3) of the parent 1,3,4-oxadiazole. The presence of two electronegative nitrogen atoms deactivates the ring, making electrophilic substitution difficult in the ring at the C2- and C5-positions. From a medicinal chemistry point of view, it is a very important molecule because it is a surrogate of carboxylic acids, esters, and carboxamides and displays a wide spectrum of pharmacological activities.
使用1,3,4-Oxadiazole has therapeutic potential with antibacterial, anti-mycobacterial, antitumor, anti-viral and antioxidant activity.
調製方法
製造方法A solution of potassium hydroxide (4 pellets) was made in absolute ethanol (40ml) & poured into a round bottom flask. 10g of prepared hydrazide and 10ml of carbon disulphide was added in the round bottom flask. Condenser was adjusted and allowed to reflux for 6-8 hours. Reaction progress was checked at regular intervals by using TLC procedure with the use of varying ratio of n-hexane & ethyl acetate. As the reaction got completed, 20ml of chilled distilled water and a very small amount of dil. Sulfuric acid (H2SO4) to maintain the pH 2-3 in order to remove un-reacted base. Solid precipitates were obtained on vigorous shaking and filtered. Product was dried, collected &calculated.
上流・下流製品情報
上流原料
サプライヤー26 社
関連反応
関連ノート
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