571172
[4-(1-Pyrrolidinylmethyl)phenyl]magnesium bromide solution
0.25 M in THF
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About This Item
Linear Formula:
C6H4CH2NC4H8MgBr
CAS Number:
Molecular Weight:
264.44
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
reaction suitability
reaction type: Grignard Reaction
concentration
0.25 M in THF
bp
65 °C
density
0.916 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
Br[Mg]c1ccc(CN2CCCC2)cc1
InChI
1S/C11H14N.BrH.Mg/c1-2-6-11(7-3-1)10-12-8-4-5-9-12;;/h2-3,6-7H,4-5,8-10H2;1H;/q;;+1/p-1
InChI key
SMCUOBSDAGTZFC-UHFFFAOYSA-M
Application
[4-(1-Pyrrolidinylmethyl)phenyl]magnesium bromide can be used:
- In the combinatorial preparation of rosamine derivatives, which are applicable as fluorescent probes in monitoring cellular glutathione (GSH) levels.
- In the synthesis of 4,5-disubstituted-2-aminoimidazole−triazole derivatives having antibiofilm activity.
Legal Information
Product of Rieke® Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3
Target Organs
Central nervous system, Respiratory system
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
1.4 °F - closed cup
Flash Point(C)
-17 °C - closed cup
Regulatory Information
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Find documentation for the products that you have recently purchased in the Document Library.
Evaluation of 4, 5-Disubstituted-2-Aminoimidazole--Triazole Conjugates for Antibiofilm/Antibiotic Resensitization Activity Against MRSA and Acinetobacter baumannii
Su Z, et al.
ChemMedChem, 6(12), 2243-2251 (2011)
Combinatorial rosamine library and application to in vivo glutathione probe
Ahn Y, et al.
Journal of the American Chemical Society, 129(15), 4510-4511 (2007)
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