Skip to Content
Merck
All Photos(2)

Documents

190705

Sigma-Aldrich

Ethyl 4-chloro-4-oxobutyrate

94%

Synonym(s):

Ethyl succinyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

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

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

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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Enantioselective Strecker-type reaction promoted by polymer-supported bifunctional catalyst.
Nogami H, et al.
Tetrahedron Letters, 42(2), 279-283 (2001)
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)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service