推荐产品
等級
technical
品質等級
化驗
≥90% (GC)
形狀
liquid
折射率
n20/D 1.413 (lit.)
bp
56-57 °C/8 mmHg (lit.)
密度
0.848 g/mL at 25 °C (lit.)
SMILES 字串
CN(C)C(OC(C)(C)C)OC(C)(C)C
InChI
1S/C11H25NO2/c1-10(2,3)13-9(12(7)8)14-11(4,5)6/h9H,1-8H3
InChI 密鑰
DBNQIOANXZVWIP-UHFFFAOYSA-N
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應用
N,N-二甲基甲酰胺二-叔-丁基缩醛可用于制备以下物质:
- (S)-2-(1-叔-丁氧基羰基-2- {4- [2-(5-甲基-2-苯基恶唑-4-基)乙氧基]苯基}乙氨基)苯甲酸甲酯
- 3-O-叔-丁基吗啡
- 吡咯和吲哚羧酸的叔-丁酯
其他說明
综述;叔-丁酯的合成。
訊號詞
Warning
危險分類
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
95.0 °F - closed cup
閃點(°C)
35 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
Synthesis, 135-135 (1983)
Convenient synthesis of pyrrole-and indolecarboxylic acid tert-butylesters.
Synthetic Communications, 34(20), 3691-3695 (2004)
Journal of medicinal chemistry, 25(10), 1264-1266 (1982-10-01)
3-O-tert-Butylmorphine (5) was prepared from 6-O-acetylmorphine (3) via alkylation with N,N-dimethylformamide di-tert-butyl acetal, followed by hydrolytic removal of the 3-(dimethylamino)-2-propenoate group. The same process was used to prepare the tert-butyl ether of levorphanol (6), (-)-3-tert-butoxy-N-methylmorphinan (8). Both 5 and 8
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 46(10), 1719-1726 (2005-10-06)
The goal of this study was to synthesize and evaluate in vivo the peroxisome proliferator-activated receptor-gamma (PPARgamma) agonist (11)C-GW7845 ((S)-2-(1-carboxy-2-{4-[2-(5-methyl-2-phenyloxazol-4-yl)ethoxy]phenyl}ethylamino)benzoic acid methyl ester) ((11)C-compound 1). PPARgamma is a member of a family of nuclear receptors that plays a central role
Tetrahedron, 35, 1675-1675 (1979)
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