All Photos(2)
Synonym(s):
Ethyl succinyl chloride
Linear Formula:
ClCOCH2CH2CO2C2H5
CAS Number:
Molecular Weight:
164.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
94%
form
liquid
refractive index
n20/D 1.437 (lit.)
bp
88-90 °C/11 mmHg (lit.)
density
1.155 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CCOC(=O)CCC(Cl)=O
InChI
1S/C6H9ClO3/c1-2-10-6(9)4-3-5(7)8/h2-4H2,1H3
InChI key
IXZFDJXHLQQSGQ-UHFFFAOYSA-N
Related Categories
Application
Ethyl 4-chloro-4-oxobutyrate was used in the synthesis of:
- polymer-supported bifunctional catalyst
- succinimidyl ester of benzo(a)pyrene
- succinate prodrugs of curcuminoids
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Wisut Wichitnithad et al.
Molecules (Basel, Switzerland), 16(2), 1888-1900 (2011-02-24)
A novel series of succinyl derivatives of three curcuminoids were synthesized as potential prodrugs. Symmetrical (curcumin and bisdesmethoxycurcumin) and unsymmetrical (desmethoxycurcumin) curcuminoids were prepared through aldol condensation of 2,4-pentanedione with different benzaldehydes. Esterification of these compounds with a methyl or
Surface plasmon resonance detection of endocrine disruptors using immunoprobes based on self-assembled monolayers.
Gobi KV, et al.
Sensors and Actuators B, Chemical, 108(1), 784-790 (2005)
Enantioselective Strecker-type reaction promoted by polymer-supported bifunctional catalyst.
Nogami H, et al.
Tetrahedron Letters, 42(2), 279-283 (2001)
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