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361933

Sigma-Aldrich

2-Benzimidazolepropionic acid

97%

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About This Item

Empirical Formula (Hill Notation):
C10H10N2O2
CAS Number:
Molecular Weight:
190.20
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

229-231 °C (dec.) (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)CCc1nc2ccccc2[nH]1

InChI

1S/C10H10N2O2/c13-10(14)6-5-9-11-7-3-1-2-4-8(7)12-9/h1-4H,5-6H2,(H,11,12)(H,13,14)

InChI key

XYWJNTOURDMTPI-UHFFFAOYSA-N

General description

2-Benzimidazolepropionic acid is a 2-(4-thiazolyl)benzimidazole analog.[1] 2-Benzimidazolepropionic acid is a 2-substituted benzimidazole ligand and its dissociation constant has been evaluated.[2] 2-Benzimidazolepropionic acid is reported to possess active antimarial activity.

Application

2-Benzimidazolepropionic acid is suitable reagent for use in the method of generation of monoclonal antibodies against very small drug hapten, 5-benzimidazolecarboxylic acid by in vivo immunisation method and an in vitro immunisation procedure.[1] It may be used in the synthesis of cytidine derivatives.[3]

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Christine M Crane et al.
ChemMedChem, 3(1), 91-101 (2007-11-23)
The enzymes of the non-mevalonate pathway for isoprenoid biosynthesis are attractive targets for the development of novel drugs against malaria and tuberculosis. This pathway is used exclusively by the corresponding pathogens, but not by humans. A series of water-soluble, cytidine-based
A Potentiometric Study of 2-Substituted Benzimidazole Ligands1.
Lane TJ and Daly JM.
Journal of the American Chemical Society, 81(12), 2953-2955 (1959)
W Kuźmierkiewicz et al.
Die Pharmazie, 40(7), 462-464 (1985-07-01)
Condensation reactions of 3-(1H-benzimidazole-2)propanoic acid (procodazol) with aromatic aldehydes were carried out resulting in lactam and acid derivatives. Basing on the spectral studies (MS, NMR) it was found that in the reaction the hydrogen atoms of the 3-methylene group of
G Martinez et al.
Medicina cutanea ibero-latino-americana, 16(3), 197-200 (1988-01-01)
We are commenting on a case of cutaneous mycobacteriosis (M. chelonei) in an asthmatic 60-year-old patient under continuous steroid treatment, who months after an accidental trauma on his hand, developed painful papular lesions, located over the trauma scar, and on
E Moran et al.
Journal of immunological methods, 271(1-2), 65-75 (2002-11-26)
Drug-specific monoclonal antibodies (MAbs) were produced against the very small drug hapten (162.15 Da), 5-benzimidazolecarboxylic acid, an analogue of 2-(4-Thiazolyl)benzimidazole (TBZ) but lacking the thiol group. TBZ is widely used as a broad-spectrum anthelmintic in various animal species and humans

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