Thermo Scientific Chemicals

1,1'-Carbonyldiimidazole, 97%, Thermo Scientific Chemicals

Catalog number: A14688.09
10 g, Each
Thermo Scientific Chemicals

1,1'-Carbonyldiimidazole, 97%, Thermo Scientific Chemicals

Catalog number: A14688.09
10 g, Each
Quantity
Catalog number: A14688.09
also known as A14688-09
Price (USD)
Price: 55.00
Online price: 46.65
Your price:
Quantity
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Chemical Identifiers

CAS
530-62-1
IUPAC Name
1-(1H-imidazole-1-carbonyl)-1H-imidazole
Molecular Formula
C7H6N4O
InChI Key
PFKFTWBEEFSNDU-UHFFFAOYSA-N
SMILES
O=C(N1C=CN=C1)N1C=CN=C1
Appearance (Color)
White to cream
Form
Crystals or powder or crystalline powder
Assay (Non-aqueous acid-base Titration)
≥96.0 to ≤104.0% (total imidazole content)
Solution Test
5% solution in DMF is clear
Identification (FTIR)
Conforms

Description

Peptide coupling reagent1,1'-Carbonyldiimidazole acts as a coupling reagent and utilized for coupling of amino acids in order to prepare peptide in organic synthesis. It is also used in the preparation of beta-keto sulfones, sulfoxides and beta-enamino acid derivatives. It is used to convert alcohols and amines into carbamates, esters, and ureas. It is involved in the preparation of formylized imidazole by reaction with formic acid. Further, it is used in the synthesis of dipolar polyamides compounds. In addition to this, it is considered as an equivalent of phosgene and used to prepare asymmetric bis alkyl carbonate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Peptide coupling reagent1,1′-Carbonyldiimidazole acts as a coupling reagent and utilized for coupling of amino acids in order to prepare peptide in organic synthesis. It is also used in the preparation of beta-keto sulfones, sulfoxides and beta-enamino acid derivatives. It is used to convert alcohols and amines into carbamates, esters, and ureas. It is involved in the preparation of formylized imidazole by reaction with formic acid. Further, it is used in the synthesis of dipolar polyamides compounds. In addition to this, it is considered as an equivalent of phosgene and used to prepare asymmetric bis alkyl carbonate.

Solubility
Soluble in dimethylformamide.

Notes
Store in a cool place. Incompatible with water, strong acids, strong oxidizing agents, strong bases and amines.
RUO – Research Use Only

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