Cyclopropylmagnesium bromide
Cyclopropylmagnesium bromide Basic information
- Product Name:
- Cyclopropylmagnesium bromide
- Synonyms:
-
- Cyclopropylmagnesium bromide solution( 1.0 M solution in THF)
- Cyclopropylmagnesium bromide solution( 0.5 M solution in THF)
- Bromocyclopropylmagnesium
- Cyclopropylbromomagnesium
- Cyclopropylmagnesium bromide, ca 0.5M in THF
- Cyclopropylmagnesium Bromide (15% in Tetrahydrofuran, ca. 1mol/L)
- cyclopropylmagnesium bromide solution
- Cyclopropylmagnesium bromide,0.5M solution inTHF
- CAS:
- 23719-80-4
- MF:
- C3H5BrMg
- MW:
- 145.28
- EINECS:
- 472-500-0
- Product Categories:
-
- Grignard Reagent
- 25mL Sure/Seal Reagents
- Cyclopropanes
- Grignard Reagents
- Chemical Synthesis
- Organometallic Reagents
- Grignard Reagents & Alkyl Metals
- Simple 3-Membered Ring Compounds
- Synthetic Organic Chemistry
- Alkyl
- Grignard Reagents
- Organometallic Reagents
- Mol File:
- 23719-80-4.mol
Cyclopropylmagnesium bromide Chemical Properties
- Boiling point:
- 65 °C
- Density
- 0.968 g/mL at 25 °C
- Flash point:
- 65°C
- storage temp.
- 2-8°C
- form
- Turbid Liquid
- color
- Yellow to green
- Water Solubility
- Soluble in water (17 mg/ml), (25°C). Soluble in organic solvents.
- Sensitive
- Air & Moisture Sensitive
- InChIKey
- QUPLLJGAJVXXBW-UHFFFAOYSA-M
- CAS DataBase Reference
- 23719-80-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- F,Xi,C
- Risk Statements
- 11-14-19-36/37/38-40-37-34
- Safety Statements
- 16-26-45-36/37/39
- RIDADR
- UN 3399 4.3/PG 2
- WGK Germany
- 1
- HazardClass
- 4.3
- PackingGroup
- II
- HS Code
- 29319090
MSDS
- Language:English Provider:SigmaAldrich
Cyclopropylmagnesium bromide Usage And Synthesis
Chemical Properties
Clear colorless solution
Uses
It often acts as the starting nutrient mix for dropout studies where fermentation conditions required the absence of one or more essential amino acids. For classifying Yeasts based on colonial characteristics and cell morphology.
Uses
Cyclopropylmagnesium bromide solution has been used in Grignard reaction that finds application as the key step in the preparation of aminopropylindenes, a chemotype of oxidosqualene cyclase (OSC) inhibitors from Grundmann′s ketone. It can react with trimethylborate to form cyclopropylboronic acid, which can undergo Suzuki-type coupling reactions with different aryl, and heteroaryl bromides to form the cyclopropyl adducts.
Uses
Grignard reagent in greener solvent, 2-methyltetrahydrofuran (2-MeTHF)
2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry
General Description
This product, 1.0 M in 2-methyltetrahydrofuran aligns with Safer Solvents and Auxiliaries, Use of Renewable Feedstocks and Inherently Safer Chemistry for Accident Prevention.
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Cyclopropylmagnesium bromide(23719-80-4)Related Product Information
- Dicyclopropane methylamine
- Allyl bromide
- ETHYNYLMAGNESIUM BROMIDE
- Sodium bromate
- Ethidium bromide
- Propylthiouracil
- Cyclopropyl acetylene
- Cyclopropanecarbonitrile
- Methylmagnesium Bromide
- Cyclopropyl bromide
- Cyclopropyl methyl ketone
- Cyclopropanesulfonyl chloride
- Rocuronium bromide
- Allyl chloride
- Benzyl bromide
- Magnesium bromide
- 1,1-Bis(hydroxymethyl)cyclopropane
- ALPHA-CYCLOPROPYLBENZYL ALCOHOL