Skip to Content
Merck
All Photos(1)

Documents

472611

Sigma-Aldrich

(1,3-Dioxolan-2-ylmethyl)magnesium bromide solution

0.5 M in THF

Synonym(s):

2-[(Bromomagnesio)methyl]-1,3-dioxolane, Bromo(1,3-dioxolan-2-ylmethyl)magnesium

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H7BrMgO2
CAS Number:
Molecular Weight:
191.31
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

reaction suitability

reaction type: Grignard Reaction

concentration

0.5 M in THF

bp

65-67 °C

density

0.938 g/mL at 25 °C

SMILES string

Br[Mg]CC1OCCO1

InChI

1S/C4H7O2.BrH.Mg/c1-4-5-2-3-6-4;;/h4H,1-3H2;1H;/q;;+1/p-1

InChI key

ZDNTZRAFJZERSL-UHFFFAOYSA-M

Application

(1,3-Dioxolan-2-ylmethyl)magnesium bromide is a Grignard reagent that can be used to prepare:
  • 3-[11C]-Propionaldehyde, a key intermediate for the synthesis of radiolabeled compound [11C]SN-38, wherein SN-38 is 7-ethyl-10-hydroxy camptothecin.
  • 1-[(S)-2,2-Dimethyl-(1,3)-dioxolan-4-yl]-4-(1,3-dioxolan2-yl)-2-ol by reacting with D-glyceraldehyde, which is further used to synthesize unsaturated nucleosides.
  • A bicyclo carboxylate intermediate, which is employed in the total synthesis of spirovibsanin A.

Signal Word

Danger

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Towards the Total Synthesis of Spirovibsanin A: Total Synthesis of (pm)-5, 14-Bis-epi-spirovibsanin A
Gallen MJ and Williams CM
European Journal of Organic Chemistry, 2008(27), 4697-4705 (2008)
Synthesis and biodistribution of [11C] SN-38
Apana SM, et al.
Journal of Labelled Compounds & Radiopharmaceuticals, 53(4), 178-182 (2010)
Synthesis, Structure- Activity Relationships, and Drug Resistance of beta-d-3′-Fluoro-2′, 3′-Unsaturated Nucleosides as Anti-HIV Agents
Zhou W, et al.
Journal of Medicinal Chemistry, 47(13), 3399-3408 (2004)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service