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.
Quantity
- (1)
- (2)
- (35)
- (7)
- (1)
- (1)
- (22)
- (1)
- (4)
- (3)
- (1)
- (1)
- (58)
- (6)
- (8)
- (5)
- (1)
- (2)
- (2)
- (3)
- (1)
- (6)
- (1)
- (126)
- (15)
- (2)
- (27)
- (4)
- (9)
- (5)
- (1)
- (1)
- (1)
- (1)
- (1)
- (83)
- (3)
- (23)
- (1)
- (4)
- (2)
- (54)
- (8)
- (1)
- (2)
Molecular Weight (g/mol)
- (7)
- (4)
- (2)
- (10)
- (5)
- (1)
- (1)
- (4)
- (3)
- (4)
- (2)
- (6)
- (5)
- (5)
- (1)
- (3)
- (3)
- (3)
- (2)
- (4)
- (1)
- (7)
- (3)
- (6)
- (7)
- (1)
- (1)
- (2)
- (6)
- (5)
- (5)
- (2)
- (6)
- (4)
- (4)
- (3)
- (1)
- (1)
- (3)
- (2)
- (1)
- (1)
- (5)
- (6)
- (2)
- (4)
- (3)
- (6)
- (3)
- (1)
- (1)
- (4)
- (8)
- (4)
- (3)
- (3)
- (1)
- (1)
- (4)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (10)
- (6)
- (4)
- (7)
- (2)
- (1)
- (1)
- (1)
- (1)
- (5)
- (1)
- (1)
- (1)
- (2)
- (16)
- (2)
- (2)
- (5)
- (3)
- (1)
- (3)
- (3)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (6)
- (18)
- (2)
- (2)
- (2)
- (1)
- (1)
- (5)
- (2)
- (1)
- (2)
- (2)
- (1)
- (7)
- (11)
- (4)
- (2)
- (2)
- (1)
- (4)
- (2)
- (4)
- (2)
- (2)
- (8)
- (1)
- (2)
- (2)
- (4)
- (7)
- (3)
- (5)
- (3)
- (1)
- (1)
- (2)
- (5)
- (3)
- (2)
- (4)
- (1)
- (2)
- (6)
- (2)
- (2)
- (2)
- (1)
- (3)
- (2)
- (5)
- (4)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
- (3)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (8)
- (9)
- (4)
- (6)
- (2)
- (4)
Percent Purity
- (2)
- (1)
- (1)
- (3)
- (2)
- (17)
- (1)
- (2)
- (5)
- (3)
- (30)
- (5)
- (1)
- (16)
- (56)
- (21)
- (1)
- (22)
- (1)
- (4)
- (3)
- (2)
- (7)
- (3)
- (5)
- (3)
- (1)
- (15)
- (13)
- (99)
- (2)
- (3)
- (89)
- (3)
- (49)
- (1)
- (5)
Boiling Point
- (2)
- (1)
- (3)
- (2)
- (2)
- (3)
- (3)
- (2)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (3)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (3)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (2)
- (7)
- (3)
- (1)
- (2)
- (1)
- (3)
- (8)
- (2)
- (1)
- (1)
- (3)
- (4)
- (2)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (4)
- (5)
- (3)
- (3)
- (2)
- (4)
- (3)
- (6)
- (3)
- (4)
- (3)
- (2)
- (4)
- (2)
- (3)
- (1)
- (3)
- (2)
- (1)
- (2)
- (4)
- (2)
- (2)
- (3)
- (2)
- (1)
- (2)
- (4)
- (2)
- (1)
- (4)
- (4)
- (12)
- (9)
- (2)
- (2)
- (1)
- (2)
- (1)
- (3)
- (2)
- (3)
- (1)
- (8)
- (1)
- (2)
- (3)
- (9)
- (3)
- (4)
- (2)
- (3)
- (2)
- (6)
- (2)
- (1)
- (2)
- (3)
- (2)
- (4)
- (1)
- (3)
- (2)
- (3)
- (1)
- (1)
- (3)
- (2)
- (1)
- (2)
- (2)
- (3)
- (4)
- (7)
- (1)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (3)
- (2)
- (6)
- (2)
- (2)
- (2)
- (1)
- (1)
- (3)
- (2)
- (3)
- (2)
- (1)
Physical Form
- (2)
- (5)
- (4)
- (2)
- (4)
- (42)
- (1)
- (3)
- (2)
- (207)
- (2)
- (11)
- (4)
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eMolecules Isopropyl 6-bromohexanoate | 64135-07-5 | | 1g
Oakwood Chemical | Isopropyl 6-bromohexanoate | 1g | 537709399 | 102847 | | 64135-07-5 | | 237.137 | C9H17BrO2
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Medchemexpress LLC Acetic acid, 2-iodo-, sodium salt | 305-53-3 | 99.9% | 10 G
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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.
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513
Strem, An Ascensus Company CAS# 383-63-1. 100g. Ethyltrifluoroacetate, 99%. MFCD00000419
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CAS# 383-63-1. 100g. Ethyltrifluoroacetate, 99%. MFCD00000419. Molecular Weight: 142.08. Molecular Formula: CF3CO2C2H5. Color/form: colorless liq. Strem# 09-3270. http://www.strem.com/catalog/v/09-3270/
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eMolecules EMOLECULES INC
NC3934171 ETHYL BROMOACETATE
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eMolecules BENZYL 2-BROMOACETATE 100G
5000159017 BENZYL 2-BROMOACETATE 100G
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eMolecules BENZYL 2-BROMOACETATE 10G
5000162639 BENZYL 2-BROMOACETATE 10G
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eMolecules BENZYL BROMOACETATE 5G
5000163492 BENZYL BROMOACETATE 5G
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eMolecules TERT-BUTYL BROMOACETATE 25G
5000170648 TERT-BUTYL BROMOACETATE 25G
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eMolecules BENZYL BROMOACETATE 25G
5000224647 BENZYL BROMOACETATE 25G
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eMolecules EMOLECULES INC
5000472283 N-SUCCINIMIDYL BROMOACETATE 1G
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eMolecules EMOLECULES INC
5000491702 BENZYL 2-BROMOACETATE 25G
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eMolecules EMOLECULES INC
5000493024 BENZYL 2-BROMOACETATE 500G
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Chemscene CHEMSCENE
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5000575835 DIETHYL 2-CHLOROMALONATE 5G
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Chemscene CHEMSCENE
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5000578002 DIETHYL 2-CHLOROMALONATE 10G
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525
Medchemexpress LLC Sodium iodoacetate | 305-53-3 | MFCD00002686 | 99.9% | 1 G
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Sodium iodoacetate is identified as a specific inhibitor of GAPDH, exhibiting glycolysis inhibitory activity. It is also known to induce osteoarthritis and related pain models in experimental animals.
- Specific inhibitor of GAPDH.
- Exhibits glycolysis inhibitory activity.
- Induces osteoarthritis and related pain models in experimental animals.
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