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4-Cyanobenzoyl chloride, 98%, Thermo Scientific Chemicals
Catalog number: B24333.14
25 g, Each
Thermo Scientific Chemicals
4-Cyanobenzoyl chloride, 98%, Thermo Scientific Chemicals
Catalog number: B24333.14
25 g, Each
Quantity
Catalog number: B24333.14
also known as B24333-14
Price (USD)
Price: 340.00
Your price:
Quantity
-
Chemical Identifiers
CAS
6068-72-0
IUPAC Name
4-cyanobenzoyl chloride
Molecular Formula
C8H4ClNO
InChI Key
USEDMAWWQDFMFY-UHFFFAOYSA-N
SMILES
ClC(=O)C1=CC=C(C=C1)C#N
Specifications
Specification SheetAppearance (Color)
White to pale pink
Form
Crystals or powder or crystalline powder
Melting Point (clear melt)
65.0-72.0?C
Assay (Titration ex Chloride)
≥97.5 to ≤102.5%
Description
It is a reactant for organocatalytic tandem three component reactions of aldehyde, alkyl vinyl ketone, and amide. It is also employed as a reactant for synthesis of selective angiotensin II AT2 receptor agonists with reduced CYP 450 inhibition, allosteric glucokinase activators, hydantoin derivatives with antiproliferative activity, thiohydantoins and P2X7 receptor antagonists.
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
It is a reactant for organocatalytic tandem three component reactions of aldehyde, alkyl vinyl ketone, and amide. It is also employed as a reactant for synthesis of selective angiotensin II AT2 receptor agonists with reduced CYP 450 inhibition, allosteric glucokinase activators, hydantoin derivatives with antiproliferative activity, thiohydantoins and P2X7 receptor antagonists.
Solubility
Reacts with water.
Notes
Store under dry inert gas. Keep away from moisture, oxidizing agents, acids, bases, active metals, amines and alcohols.
It is a reactant for organocatalytic tandem three component reactions of aldehyde, alkyl vinyl ketone, and amide. It is also employed as a reactant for synthesis of selective angiotensin II AT2 receptor agonists with reduced CYP 450 inhibition, allosteric glucokinase activators, hydantoin derivatives with antiproliferative activity, thiohydantoins and P2X7 receptor antagonists.
Solubility
Reacts with water.
Notes
Store under dry inert gas. Keep away from moisture, oxidizing agents, acids, bases, active metals, amines and alcohols.
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