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About This Item
Linear Formula:
CH3CH2CHClCOOH
CAS Number:
Molecular Weight:
122.55
Beilstein:
1720944
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
≥97.0% (GC)
refractive index
n20/D 1.439
bp
90-92 °C/12 mmHg (lit.)
density
1.190 g/mL at 20 °C (lit.)
SMILES string
CCC(Cl)C(O)=O
InChI
1S/C4H7ClO2/c1-2-3(5)4(6)7/h3H,2H2,1H3,(H,6,7)
InChI key
RVBUZBPJAGZHSQ-UHFFFAOYSA-N
Application
2-Chlorobutyric acid was used in the synthesis of 2-hydroxy-5-hexenyl 2-chlorobutyrate ester.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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García et al.
Biochemical engineering journal, 5(3), 185-190 (2000-06-01)
An esterification process was developed for the direct synthesis of 2-hydroxy-5-hexenyl 2-chlorobutyrate ester from 2-chlorobutyric acid by using the epoxide 1,2-epoxy-5-hexene and Mucor miehei immobilised lipase as the biocatalyst in a batch reactor. The effect of temperature, catalyst concentration, and
Khatereh Bahrpaima et al.
Biomolecules, 9(8) (2019-08-23)
In this work, 1-carboxypropyled (1-CPRLS) and 5-carboxypentyled lignosulfonates (5-CPELS) were synthesized using 2-chlorobutanoic acid and 6-chlorohexanoic acid as carboxylate group donors via SN1 and SN2 mechanisms, respectively. 1-Carboxypropyl and 5-carboxypentyl lignosulfonates with the charge densities of -3.45 and -2.94 meq
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