571156
[3-(4-吗啉甲基)苯基]溴化镁 溶液
0.25 M in THF
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关于此项目
线性分子式:
C6H4CH2NOC4H8MgBr
化学文摘社编号:
分子量:
280.44
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
InChI
1S/C11H14NO.BrH.Mg/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12;;/h1-2,4-5H,6-10H2;1H;/q;;+1/p-1
SMILES string
Br[Mg]c1cccc(CN2CCOCC2)c1
InChI key
UAYUGBXOBYFKNG-UHFFFAOYSA-M
reaction suitability
reaction type: Grignard Reaction
concentration
0.25 M in THF
bp
65 °C (lit.)
density
0.926 g/mL at 25 °C (lit.)
functional group
ether
storage temp.
2-8°C
Application
[3-(4-Morpholinylmethyl)phenyl]magnesium bromide is a Grignard reagent that can be used as:
- A reagent in the synthesis of 6-((2-(2-chloroacetamido)ethyl)(methyl)amino)-9-(3-(morpholinomethyl)phenyl)-3H-xanthen-3-iminium (CDy5), a fluorescent chemical probe utilized in imaging neural stem/progenitor cells (NSPCs).
- A starting material to prepare 3-(4-morpholinylmethyl)phenol by direct oxidation using compressed air.
Legal Information
Rieke® Metals, Inc. 产品 ®Rieke Metals, Inc. 的注册商标
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
1.4 °F - closed cup
flash_point_c
-17 °C - closed cup
法规信息
新产品
此项目有
A fluorescent probe for imaging symmetric and asymmetric cell division in neurosphere formation
Y Seong-Wook, et al.
Chemical Communications (Cambridge, England), 50(56), 7492-7494 (2014)
Continuous-Flow Synthesis of Functionalized Phenols by Aerobic Oxidation of Grignard Reagents
He Zhi and Jamison TF
Angewandte Chemie (International Edition in English), 53(13), 3353-3357 (2014)
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