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190705

Sigma-Aldrich

Ethyl 4-chloro-4-oxobutyrate

94%

Synonym(s):

Ethyl succinyl chloride

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25 G
$135.00
100 G
$354.00

$135.00

Estimated to ship on13 April 2025

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25 G
$135.00
100 G
$354.00

About This Item

Linear Formula:
ClCOCH2CH2CO2C2H5
CAS Number:
14794-31-1
Molecular Weight:
164.59
EC Number:
238-855-9
MDL number:
MFCD00000751
UNSPSC Code:
12352100
PubChem Substance ID:
24851457
NACRES:
NA.22

$135.00

Estimated to ship on13 April 2025

Request a Bulk Order

Quality Level

100

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.)

functional group

acyl chloride
ester

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[1]
  • succinimidyl ester of benzo(a)pyrene[2]
  • succinate prodrugs of curcuminoids[2]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

183.2 °F - closed cup

Flash Point(C)

84 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8405
STBL4620
STBH7644
STBD3039V
STBD0021V

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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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