推荐产品
化驗
≥99.99% trace metals basis
形狀
solid
反應適用性
reaction type: click chemistry
溶解度
soluble 65 g/L at 20 °C (completely)
SMILES 字串
[Na]N=[N+]=[N-]
InChI
1S/N3.Na/c1-3-2;/q-1;+1
InChI 密鑰
PXIPVTKHYLBLMZ-UHFFFAOYSA-N
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應用
Efficient 1,4-addition of azide to a,ß-unsaturated aldehydes in the presence of tertiary amines.
Catalyst for:
Reagent for synthesis of
Involved in regioselective synthesis of prianosin B
Catalyst for:
- Oxidative decarboxylation
- Michael addition reactions
Reagent for synthesis of
- Blue fluorescent copolymers
- Metal phosphonates
- Arenes via aminations
Involved in regioselective synthesis of prianosin B
訊號詞
Danger
危險分類
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2 Oral
標靶器官
Brain
安全危害
儲存類別代碼
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Synthetic Communications, 37, 1027-1027 (2007)
Xiaohua Sun et al.
Organic letters, 9(22), 4495-4498 (2007-10-04)
A novel intermolecular cross-double-Michael addition between nitro and carbonyl activated olefins has been developed through Lewis base catalysis. The reaction took place with a large group of beta-alkyl nitroalkenes and alpha,beta-unsaturated ketone/esters, producing an allylic nitro compound in good to
Y. Wada, et al.,
Tetrahedron, 65, 1059-1062 (2009)
H. Chen, et al.,
Macromolecules, 43, 3613-3623 (2010)
G. I. Borodkin, et al.,
Russ. J. Org. Chem., 40, 1541-1542 (2004)
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