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Sigma-Aldrich

[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

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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