CAS 14337-43-0

Ethyl 2-chloro-2-(hydroxyimino)acetate

Description:

Ethyl 2-chloro-2-(hydroxyimino)acetate, with the CAS number 14337-43-0, is an organic compound characterized by its ester functional group and the presence of a chloro and a hydroxyimino substituent. This compound typically appears as a colorless to pale yellow liquid and is soluble in organic solvents. Its molecular structure features a chloro group attached to a carbon atom that is also bonded to a hydroxyimino group, which contributes to its reactivity and potential applications in organic synthesis. Ethyl 2-chloro-2-(hydroxyimino)acetate can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it valuable in the synthesis of other chemical entities. The presence of the hydroxyimino group may also impart certain biological activities, although specific biological properties would require further investigation. As with many chemical substances, proper handling and safety precautions are essential due to potential hazards associated with its reactivity and toxicity.

Formula: C₄H₆ClNO₃

InChI: InChI=1S/C4H6ClNO3/c1-2-9-4(7)3(5)6-8/h8H,2H2,1H3

InChI key: InChIKey=UXOLDCOJRAMLTQ-UHFFFAOYSA-N

SMILES: C(C(=NO)Cl)(OCC)=O

Synonyms:

• (Carbethoxy)chloroformaldoxime
• (Chloro)(hydroxyimino)acetic acid ethyl ester
• (Ethoxycarbonyl)formohydroxamoyl chloride
• (Ethoxycarbonyl)hydroxamic acid chloride
• (Z)-ethyl 2-chloro-2-(hydroxyimino)acetate
• 2-Chloro-2-(hydroxyimino)acetic acid ethyl ester
• 2-Chloro-2-hydroxyiminoacetic acid ethyl ester
• Acetic acid, 2-chloro-2-(hydroxyimino)-, ethyl ester
• Acetic acid, chloro(hydroxyimino)-, ethyl ester
• Ethyl (chloroximino)glyoxylate
• Ethyl 2-chloro-2-hydroxyiminoacetate
• Ethyl Chlorooximidoacetate
• Ethyl chloro(hydroxyimino)acetate
• Ethyl chloro(hydroxyimino)ethanoate
• Ethyl chloro(oximido)acetate
• Ethyl chloro(oximino)acetate
• Ethyl chloroglyoxylate 2-oxime
• Ethyl chloroximidoacetate
• Ethyl oximinochloroacetate
• Glyoxylic acid, chloro-, ethyl ester, 2-oxime
• Glyoxylic acid, chloro-, ethyl ester, oxime
• ethyl (2E)-chloro(hydroxyimino)ethanoate

Ethyl 2-chloro-2-(hydroxyimino)acetate

CAS: 14337-43-0

Formula: C₄H₆ClNO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 151.5483

Ref: IN-DA0034UE

Ethyl chloro(hydroxyimino)acetate

CAS: 14337-43-0

Ethyl chloro(hydroxyimino)acetate

Formula: C₄H₆ClNO₃

Purity: 97%

Color and Shape: Pale yellow Solid-Crystals

Molecular weight: 151.54834

Ref: 54-OR14997

Ethyl chlorooximinoacetate

CAS: 14337-43-0

Formula: C₄H₆O₃NCl

Purity: ≥ 97.0%

Color and Shape: White to light pink powder

Molecular weight: 151.55

Ref: 7W-GK5362

Ethyl 2-Chloro-2-(hydroxyimino)acetate

CAS: 14337-43-0

Ethyl 2-Chloro-2-(hydroxyimino)acetate

Formula: C₄H₆ClNO₃

Purity: 97%

Molecular weight: 151.55

Ref: IN-DG2300

Ethyl 2-chloro-2-(hydroxyimino)acetate

CAS: 14337-43-0

Ethyl 2-chloro-2-(hydroxyimino)acetate is an organic compound that contains a chloride group, two oxadiazole rings, and an ethyl group. It has been shown to bind to receptors on the surface of cells and act as a competitive antagonist. It has also been shown to inhibit influenza virus growth by binding to the receptor binding site on the virus surface. Ethyl 2-chloro-2-(hydroxyimino)acetate can be made synthetically or in nature by the reaction of formaldehyde with ammonia, which produces glutamic acid and hydrogen chloride gas. This molecule is able to react with sodium carbonate in water to produce ethyl chloroformate. The molecule has been shown to have cancerous effects when injected into rats.

Formula: C₄H₆ClNO₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 151.55 g/mol

Ref: 3D-FE34373

Ethyl chlorooximinoacetate

CAS: 14337-43-0

Formula: C₄H₆ClNO₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 151.55

Ref: 10-F047343

Ethyl 2-Chloro-2-(hydroxyimino)acetate

CAS: 14337-43-0

Formula: C₄H₆ClNO₃

Purity: >99.0%(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 151.55

Ref: 3B-E0371