Skip to Content
Merck
All Photos(1)

Key Documents

20959

Sigma-Aldrich

Cesium carbonate

puriss. p.a., ≥99.0%

Synonym(s):

Carbonic acid dicesium

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
Cs2CO3
CAS Number:
Molecular Weight:
325.82
Beilstein:
4546405
EC Number:
MDL number:
UNSPSC Code:
12352301
PubChem Substance ID:
NACRES:
NA.22

grade

puriss. p.a.

Quality Level

Assay

≥99.0% (T)
≥99.0%

impurities

≤0.002% total nitrogen (N)

mp

610 °C (dec.) (lit.)

anion traces

chloride (Cl-): ≤20 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

[Cs+].[Cs+].[O-]C([O-])=O

InChI

1S/CH2O3.2Cs/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2

InChI key

FJDQFPXHSGXQBY-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Cesium carbonate is an inorganic base generally used in C, N, O-arylation and alkylation reactions. It is also used in six-membered annulation, cross-coupling, intramolecular and intermolecular cyclizations, aza-Henry reaction, Horner-Emmons cyclization, and cycloaddition reactions.

Application

Cesium carbonate, an alkali metal carbonate, is a commonly used inorganic base in organic reactions.
Synthetic applications:
  • As a catalyst to synthesize quinazoline-2,4(1H,3H)-diones from substituted 2-aminobenzonitriles and carbon dioxide.
  • As a base to synthesize cyclic carbonates using halo- or tosyl-alcohols and carbon dioxide in the absence of any transition metal or organo catalyst.
  • In combination with alkyl halide and acetonitrile, it forms an effective system for the alkylation method of phenols.

Promotes the efficient O-alkylation of alcohols to form mixed alkyl carbonates.

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Repr. 2 - STOT RE 2 Oral

Target Organs

Kidney,Adrenal gland,Testes

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Facile synthesis of alkyl phenyl ethers using cesium carbonate.
Lee J C, et al.
Synthetic Communications, 25(9), 1367-1370 (1995)
Cesium carbonate
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2016)
Cesium carbonate: a powerful inorganic base in organic synthesis.
Flessner T and Doye S.
J. Prakt. Chem., 341(2), 186-190 (1999)
Synthesis of cyclic carbonates with carbon dioxide and cesium carbonate.
Reithofer M R, et al.
Green Chemistry, 15(8), 2086-2090 (2013)
Cesium carbonate catalyzed efficient synthesis of quinazoline-2, 4 (1 H, 3 H)-diones using carbon dioxide and 2-aminobenzonitriles.
Patil Y P, et al.
Green Chemistry Letters and Reviews, 1(2), 127-132 (2008)

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