1,3,4-オキサジアゾール

1,3,4-Oxadiazole

HCID 97428CAS 288-99-3

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

1,3,4-Oxadiazole288-99-320O2F20OURNSC-122449DTXSID10182987RefChem:72245DTXCID50105478873-098-3[1,3,4]oxadiazoleOXDIAZOLEMFCD009555351-Oxa-3,4-diazacyclopentadiene
名称をさらに表示
1,3,4-オキサジアゾール
C2H2N2OUNII-20O2F20OUR1,4-OxadiazoleNSC1224491,3,4-oxadiazol1,3,4 oxadiazole1,3,4-furodiazoleSCHEMBL4867

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

実験および物理化学的性質

Chemical ClassesNitrogen Compounds -> Other Nitrogen Compounds
SpringerMaterials PropertiesSchoenflies notation
Physical DescriptionLiquid; [Merck Index]

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

安全と法規制

GHS分類

GHS Classification · 4 件

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

Hazards SummaryAn irritant; [Matrix Scientific MSDS]
Hazard Classes and CategoriesSkin Irrit. 2 (100%)

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 · 2 件

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 · 1 件

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.

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関連反応

2 件

関連ノート

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