D157805
N,N′-二甲基乙二胺
98%
别名:
DMEDA, 1,2-双(甲氨基)乙烷
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
CH3NHCH2CH2NHCH3
化学文摘社编号:
分子量:
88.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-793-3
Beilstein/REAXYS Number:
878142
MDL number:
Assay:
98%
Form:
liquid
InChI key
KVKFRMCSXWQSNT-UHFFFAOYSA-N
InChI
1S/C4H12N2/c1-5-3-4-6-2/h5-6H,3-4H2,1-2H3
SMILES string
CNCCNC
assay
98%
form
liquid
refractive index
n20/D 1.431 (lit.)
bp
119 °C (lit.)
density
0.819 g/mL at 20 °C (lit.)
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
N,N′-二甲基乙二胺可用作以下过程的配体：
- 铜催化铁氰化钾参与的芳基溴代物的氰化反应，形成相应的苄腈。
- 铜催化碳化二亚胺和异氰基乙酸酯的串联反应，形成苯并咪唑[1,5-α]咪唑。
- 1,1-二溴烯烃的氨基硫化反应，形成N-稠杂环。
- 与氯化亚铁结合，用于NH-亚砜亚胺与芳基碘化物的N-芳基化反应，形成N-芳基亚砜亚胺。
- 在叔丁醇钾存在下，它可催化未活化苯的直接C-H芳基化反应，形成相应的联芳基。
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
78.8 °F - closed cup
flash_point_c
26 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Organocatalysis in cross-coupling: DMEDA-catalyzed direct C? H arylation of unactivated benzene.
Liu W, et al.
Journal of the American Chemical Society, 132(47), 16737-16740 (2010)
Copper-catalyzed synthesis of N-fused heterocycles through regioselective 1, 2-aminothiolation of 1, 1-dibromoalkenes.
Xu H, et al.
Organic Letters, 12(16), 3704-3707 (2010)
J T Hwang et al.
Nucleic acids research, 27(19), 3805-3810 (1999-09-11)
The formal C1'-oxidation product, 2-deoxyribonolactone, is formed as a result of DNA damage induced via a variety of agents, including gamma-radiolysis and the enediyne antitumor antibiotics. This alkaline labile lesion may also be an intermediate during DNA damage induced by
Ghotas Evindar et al.
The Journal of organic chemistry, 71(5), 1802-1808 (2006-02-25)
A general method for the formation of benzoxazoles via a copper-catalyzed cyclization of ortho-haloanilides is reported. This approach complements the more commonly used strategies for benzoxazole formation which require 2-aminophenols as substrates. The reaction involves an intramolecular C-O cross-coupling of
Kim A Lennox et al.
Oligonucleotides, 16(1), 26-42 (2006-04-06)
A wide variety of modified oligonucleotides have been tested as antisense agents. Each chemical modification produces a distinct profile of potency, toxicity, and specificity. Novel cationic phosphoramidate-modified antisense oligonucleotides have been developed recently that have unique and interesting properties. We
商品
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持