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Alpha-halocarboxylic acids and derivatives

Organic compounds that contain a carboxyl group bonded to a halogen group in the alpha position; halogen groups consist of one or more halogen atoms (F, Cl, B, I, At). Includes compounds that are derived from alpha-halocarboxylic acids.
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1

Ethyl Dibromofluoroacetate 97.0+%, TCI America™

CAS: 565-53-7 Molecular Formula: C4H5Br2FO2 Molecular Weight (g/mol): 263.89 MDL Number: MFCD00042068 InChI Key: COYRDMUQLSIAEX-UHFFFAOYSA-N Synonym: ethyl dibromofluoroacetate,dibromofluoroacetic acid ethyl ester,ethyldibromofluoroacetate,2,2-dibromo-1-ethoxy-2-fluoroethan-1-one,acmc-1aqw2,ethyl 2,2-dibromo-2-fluoracetate,ethyl 2,2-dibromo-2-fluoro-acetate PubChem CID: 2737168 IUPAC Name: ethyl 2,2-dibromo-2-fluoroacetate SMILES: CCOC(=O)C(F)(Br)Br

PubChem CID 2737168
CAS 565-53-7
Molecular Weight (g/mol) 263.89
MDL Number MFCD00042068
SMILES CCOC(=O)C(F)(Br)Br
Synonym ethyl dibromofluoroacetate,dibromofluoroacetic acid ethyl ester,ethyldibromofluoroacetate,2,2-dibromo-1-ethoxy-2-fluoroethan-1-one,acmc-1aqw2,ethyl 2,2-dibromo-2-fluoracetate,ethyl 2,2-dibromo-2-fluoro-acetate
IUPAC Name ethyl 2,2-dibromo-2-fluoroacetate
InChI Key COYRDMUQLSIAEX-UHFFFAOYSA-N
Molecular Formula C4H5Br2FO2
2

Iodoacetic acid, sodium salt, 99%

CAS: 305-53-3 Molecular Formula: C2H2INaO2 Molecular Weight (g/mol): 207.93 MDL Number: MFCD00002686 InChI Key: AGDSCTQQXMDDCV-UHFFFAOYSA-M Synonym: sodium iodoacetate,iodoacetic acid sodium salt,acetic acid, iodo-, sodium salt,sodium 2-iodoacetate,sodium monoiodoacetate,iodoacetate, sodium salt,sodium iodacetate,iodoacetic acid, sodium salt,unii-07814f2qri,ccris 9232 PubChem CID: 5239 IUPAC Name: sodium;2-iodoacetate SMILES: C(C(=O)[O-])I.[Na+]

PubChem CID 5239
CAS 305-53-3
Molecular Weight (g/mol) 207.93
MDL Number MFCD00002686
SMILES C(C(=O)[O-])I.[Na+]
Synonym sodium iodoacetate,iodoacetic acid sodium salt,acetic acid, iodo-, sodium salt,sodium 2-iodoacetate,sodium monoiodoacetate,iodoacetate, sodium salt,sodium iodacetate,iodoacetic acid, sodium salt,unii-07814f2qri,ccris 9232
IUPAC Name sodium;2-iodoacetate
InChI Key AGDSCTQQXMDDCV-UHFFFAOYSA-M
Molecular Formula C2H2INaO2
3
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Ethyl dibromofluoroacetate, 97%

CAS: 565-53-7 Molecular Formula: C4H5Br2FO2 Molecular Weight (g/mol): 263.89 MDL Number: MFCD00042068 InChI Key: COYRDMUQLSIAEX-UHFFFAOYSA-N Synonym: ethyl dibromofluoroacetate,dibromofluoroacetic acid ethyl ester,ethyldibromofluoroacetate,2,2-dibromo-1-ethoxy-2-fluoroethan-1-one,acmc-1aqw2,ethyl 2,2-dibromo-2-fluoracetate,ethyl 2,2-dibromo-2-fluoro-acetate PubChem CID: 2737168 IUPAC Name: ethyl 2,2-dibromo-2-fluoroacetate SMILES: CCOC(=O)C(F)(Br)Br

PubChem CID 2737168
CAS 565-53-7
Molecular Weight (g/mol) 263.89
MDL Number MFCD00042068
SMILES CCOC(=O)C(F)(Br)Br
Synonym ethyl dibromofluoroacetate,dibromofluoroacetic acid ethyl ester,ethyldibromofluoroacetate,2,2-dibromo-1-ethoxy-2-fluoroethan-1-one,acmc-1aqw2,ethyl 2,2-dibromo-2-fluoracetate,ethyl 2,2-dibromo-2-fluoro-acetate
IUPAC Name ethyl 2,2-dibromo-2-fluoroacetate
InChI Key COYRDMUQLSIAEX-UHFFFAOYSA-N
Molecular Formula C4H5Br2FO2
4
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Ethyl chloroacetate, 99%

CAS: 105-39-5 MDL Number: MFCD00000932 InChI Key: VEUUMBGHMNQHGO-UHFFFAOYSA-N Synonym: ethyl chloroacetate,ethyl chloracetate,ethyl monochloroacetate,acetic acid, chloro-, ethyl ester,chloroacetic acid ethyl ester,ethyl monochloracetate,ethyl chloroethanoate,ethyl alpha-chloroacetate,2-chloroacetic acid ethyl ester,unii-6h07teh4tf PubChem CID: 7751 IUPAC Name: ethyl 2-chloroacetate SMILES: CCOC(=O)CCl

PubChem CID 7751
CAS 105-39-5
MDL Number MFCD00000932
SMILES CCOC(=O)CCl
Synonym ethyl chloroacetate,ethyl chloracetate,ethyl monochloroacetate,acetic acid, chloro-, ethyl ester,chloroacetic acid ethyl ester,ethyl monochloracetate,ethyl chloroethanoate,ethyl alpha-chloroacetate,2-chloroacetic acid ethyl ester,unii-6h07teh4tf
IUPAC Name ethyl 2-chloroacetate
InChI Key VEUUMBGHMNQHGO-UHFFFAOYSA-N
5

Medchemexpress LLC Acetic acid, 2-iodo-, sodium salt | 305-53-3 | 99.9% | 10 G
SDP

Sodium iodoacetate is a specific inhibitor of GAPDH and exhibits glycolysis inhibitory activity. It can also induce osteoarthritis and related pain models in experimental animals.

  • Specific inhibitor of GAPDH.
  • Has glycolysis inhibitory activity.
  • Can induce osteoarthritis and related pain models in experimental animals.
  • Useful for research involving GAPDH inhibition.
  • Applicable in studies related to glycolysis inhibition.
  • Can be used to establish osteoarthritis and pain models in experimental animals.

ENCOMPASS_PREFERRED
6

Medchemexpress LLC Acetic acid, 2-iodo-, sodium salt | 305-53-3 | 579524 | 99.9% | 25 G
SDP

Sodium iodoacetate is a specific inhibitor of GAPDH and has glycolysis inhibitory activity. In addition, sodium iodoacetate can induce osteoarthritis and related pain models in experimental animals.

  • Specific inhibitor of GAPDH.
  • Exhibits glycolysis inhibitory activity.
  • Can induce osteoarthritis and related pain models in experimental animals.

ENCOMPASS_PREFERRED