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品質等級
化驗
98%
mp
190-192 °C (lit.)
官能基
nitro
SMILES 字串
NS(=O)(=O)c1ccccc1[N+]([O-])=O
InChI
1S/C6H6N2O4S/c7-13(11,12)6-4-2-1-3-5(6)8(9)10/h1-4H,(H2,7,11,12)
InChI 密鑰
GNDKYAWHEKZHPJ-UHFFFAOYSA-N
應用
Reactant involved in synthesis of:
Reactant involved in intermolecular amination of allyl alcohols
- Cyclic nitrogen compounds via intramolecular hydroamination
- Pentacyclic lycopodium alkaloid huperzine-Q
- Pyrrolidines
- Intermolecular C-H insertion reactions
Reactant involved in intermolecular amination of allyl alcohols
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
Chemical & pharmaceutical bulletin, 48(10), 1570-1576 (2000-10-25)
Total synthesis of spider toxins HO-416b (1) and Agel-489 (2) was accomplished using the 2-nitrobenzenesulfonamide (Ns) group as both a protecting and activating group. In this strategy, the C-N bonds were constructed by alkylation of sulfonamides with alkyl halides or
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