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品質等級
化驗
96%
mp
129-132 °C (lit.)
SMILES 字串
O=C1NCCN1
InChI
1S/C3H6N2O/c6-3-4-1-2-5-3/h1-2H2,(H2,4,5,6)
InChI 密鑰
YAMHXTCMCPHKLN-UHFFFAOYSA-N
基因資訊
human ... EPHX2(2053)
mouse ... Ephx2(13850)
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應用
用于合成以下物质的反应物：
反应物用于：
- 来源于非手性前体的手性微孔材料
- 通过微波辅助钯催化羰基化，合成芳基和杂芳基 N-酰基脲
- 一种高水溶性肽基人嗜中性粒细胞弹性蛋白酶抑制剂
- 通过氰基乙酰化合成杂环，用于抗菌应用
反应物用于：
- 使用杂芳族甲苯磺酸酯，Pd-催化的 C-N 键形成
- 活化烯烃的氧化酰胺化
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - STOT RE 2
標靶器官
Thyroid
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
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
Mette L H Mantel et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(18), 5437-5442 (2010-04-09)
A protocol for the palladium(0)-catalyzed amidation of heteroaromatic tosylates was successfully developed. The methodology proved to be effective for a variety of heteroaryl tosylates including the pyridine, pyrimidine, quinoline and quinoxaline ring systems. Successful carbon-nitrogen bond formation with these heteroaryl
Oxidative amidation of activated alkenes using Pd(OAc)2 as a catalyst precursor
X. Liu and K. K. Hii,
European Journal of Organic Chemistry, 27, 5181-5189 (2010)
Yasunao Inoue et al.
Bioorganic & medicinal chemistry, 17(21), 7477-7486 (2009-10-09)
A series of peptide-based transition-state human neutrophil elastase (HNE) inhibitors with N-terminal acidic moieties were synthesized and their inhibitory activity against HNE was evaluated both in vitro and in vivo. Our results show that compounds containing cyclic amide bridged acidic
Synthesis and antimicrobial activity of new heterocycles obtained using cyanoacetylation
Sh. M. Abu-Bakr, et al.,
Pharmaceutical Chemistry Journal, 44, 433-437 (2010)
New Synthesis of Aryl and Heteroaryl N-Acylureas via Microwave-Assisted Palladium-Catalyzed Carbonylation
D. Liptrot, et al.,
Advanced Synthesis & Catalysis, 352, 2183-2188 (2010)
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