4-Chlorobutyryl chloride, 98%, Thermo Scientific Chemicals
Element SearchElement SearchStructure SearchStructure Search
4-Chlorobutyryl chloride, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Chlorobutyryl chloride, 98%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
250 g
10 g
1000 g
ChemDexTry the chem dexTM web app
This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number A12249.30
also known as A12249-30
Price (USD)/ Each
48.70
-
Add to cart
Quantity:
250 g
Request bulk or custom format
Price (USD)/ Each
48.70
Add to cart
4-Chlorobutyryl chloride, 98%, Thermo Scientific Chemicals
Catalog numberA12249.30
Price (USD)/ Each
48.70
-
Add to cart
Chemical Identifiers
CAS4635-59-0
IUPAC Name4-chlorobutanoyl chloride
Molecular FormulaC4H6Cl2O
InChI KeyCDIIZULDSLKBKV-UHFFFAOYSA-N
SMILESClCCCC(Cl)=O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
FormLiquid
Assay (GC)≥97.5%
Refractive Index1.4595-1.4635 @ 20?C
4-Chlorobutyryl chloride (4-CBCl) is mainly used in the production of pharmaceuticals and agrochemicals. It is used as pyrazinamide intermediate.

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
4-Chlorobutyryl chloride (4-CBCl) is mainly used in the production of pharmaceuticals and agrochemicals. It is used as pyrazinamide intermediate.

Solubility
soluble in diethyl ether, ethanol, slightly soluble in water.

Notes
Moisture sensitive. Store under inert gas. Store away from oxidizing agent, bases,
RUO – Research Use Only

General References:

  1. Masatoshi Kakushima; Pierre Hamel, Richard Frenette; Joshua Rokach. Regioselective synthesis of acylpyrroles. J. Org. Chem. 1983, 48 (19), 3214-3219.
  2. David S. Ennis; Julie McManus; Wladyslaw Wood-Kaczmar; John Richardson; Gillian E. Smith and Alexis Carstairs. Multikilogram-Scale Synthesis of a Biphenyl Carboxylic Acid Derivative Using a Pd/C-Mediated Suzuki Coupling Approach. Org. Proc. Res. Dev. 1999, 3 (4), 248-252.