推荐产品
化驗
97%
反應適用性
reaction type: click chemistry
mp
180 °C (dec.) (lit.)
儲存溫度
2-8°C
SMILES 字串
OC(=O)c1ccc(cc1)S(=O)(=O)N=[N+]=[N-]
InChI
1S/C7H5N3O4S/c8-9-10-15(13,14)6-3-1-5(2-4-6)7(11)12/h1-4H,(H,11,12)
InChI 密鑰
OWULJVXJAZBQLL-UHFFFAOYSA-N
應用
Reactant for:
Synthesis of anti-inflammatory agents
Azide amidation
Reactions of thio acids with azides
Chemoselective sodium borohydride reduction of azides in water
Reagent for:
Photo-Stevens rearrangement
Cobalt-catalyzed synthesis of tertiary azides
Synthesis of anti-inflammatory agents
Azide amidation
Reactions of thio acids with azides
Chemoselective sodium borohydride reduction of azides in water
Reagent for:
Photo-Stevens rearrangement
Cobalt-catalyzed synthesis of tertiary azides
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
商品
Since the preparation of the first organic azide, phenyl azide, by Peter Griess in 1864 this energy-rich and versatile class of compounds has enjoyed considerable interest.
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