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190705

Sigma-Aldrich

Ethyl 4-chloro-4-oxobutyrate

94%

Synonym(s):

Ethyl succinyl chloride

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25 G
¥6,880
100 G
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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

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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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

190705-25G:
190705-VAR:
190705-100G:
190705-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8405
STBL4620
STBH7644
STBD3039V
STBD0021V

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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
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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