所有图片(1)
About This Item
经验公式（希尔记法）:
C6H9N3O2
CAS号:
分子量:
155.15
MDL编号:
UNSPSC代码:
12352005
PubChem化学物质编号:
NACRES:
NA.22
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方案
≥95%
表单
liquid
折射率
n20/D 1.508
密度
1.204 g/mL at 25 °C
储存温度
2-8°C
SMILES字符串
CON(C)C(=O)n1ccnc1
InChI
1S/C6H9N3O2/c1-8(11-2)6(10)9-4-3-7-5-9/h3-5H,1-2H3
InChI key
DOQREVDTYAHWSN-UHFFFAOYSA-N
应用
N-Methoxy-N-methyl-1H-imidazole-1-carboxamide (or N-methoxy-N-methylcarbamoylimidazole) can be used as a reagent to prepare:
- N-methoxy-N-methylcyanoformamide by reacting with trimethylsilyl cyanide.
- Esters and amides via chemoselective esterification and amidation of carboxylic acids.
- Carbamoylimidazolium iodides and their derivatives such as ureas, thioureas, carbamates, and amides upon reacting with amines, alcohols, thiols, and carboxylic acids.
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
N-Methoxy-N-methylcyanoformamide, a Highly Reactive Reagent for the Formation of β-Keto Weinreb Amides and Unsymmetrical Ketones
Nugent J and Schwartz BD
Organic Letters, 18(15), 3834-3837 (2016)
Carbamoylimidazolium and thiocarbamoylimidazolium salts: novel reagents for the synthesis of ureas, thioureas, carbamates, thiocarbamates and amides
Grzyb JA, et al.
Tetrahedron, 61(30), 7153-7175 (2005)
Chemoselective esterification and amidation of carboxylic acids with imidazole carbamates and ureas
Heller ST and Sarpong R
Organic Letters, 12(20), 4572-4575 (2010)
相关内容
Professor Heller's research focuses on mild acylation reactions using carbonylimidazole-derived reagents.
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