Indole-5-carboxylic acid - CAS 1670-81-1
Catalog: |
BB012348 |
Product Name: |
Indole-5-carboxylic acid |
CAS: |
1670-81-1 |
Synonyms: |
5-Carboxyindole; 5-Indolecarboxylic acid |
Related CAS: | 1669447-68-0 (Deleted CAS) 142396-03-0 (Indole-5-carboxylic acid, radical ion(1+))
|
IUPAC Name: | 1H-indole-5-carboxylic acid |
Description: | Indole-5-carboxylic acid (CAS# 1670-81-1) is used in the synthesis of selective D3 dopamine receptor agonists used to combat diseases such as Parkinson's. Also used in the preparation of potent ligand-efficient inhibitors of CTM-X Class A β-Lactamases which pose health threats to the public. |
Molecular Weight: | 161.16 |
Molecular Formula: | C9H7NO2 |
Canonical SMILES: | C1=CC2=C(C=CN2)C=C1C(=O)O |
InChI: | InChI=1S/C9H7NO2/c11-9(12)7-1-2-8-6(5-7)3-4-10-8/h1-5,10H,(H,11,12) |
InChI Key: | IENZCGNHSIMFJE-UHFFFAOYSA-N |
Boiling Point: | 419.6±18.0°C at 760 Torr |
Melting Point: | 208-209°C |
Purity: | ≥95% |
Density: | 1.408±0.06 g/cm3 |
Appearance: | Light beige to yellow powder |
MDL: | MFCD00005678 |
LogP: | 1.86610 |
GHS Hazard Statement: | H302 (14.29%): Harmful if swallowed [Warning Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113368390-A | Preparation of polybenzazole derivative conductive adhesion layer for nerve electrode modification | 20210618 |
CN-112390781-A | Diaryl substituted 1, 1-ethylene compound, preparation method and application | 20201118 |
WO-2021204626-A1 | Aryl and heteroaryl-carboxamide substituted heteroaryl compounds as tyk2 inhibitors | 20200406 |
WO-2021202977-A1 | Pyrrolopyrimidine amines as complement inhibitors | 20200403 |
US-2021301175-A1 | Polishing composition | 20200330 |
PMID | Publication Date | Title | Journal |
22841068 | 20120815 | Effect of organic solvents on peroxidases from rice and horseradish: prospects for enzyme based applications | Talanta |
22594259 | 20120501 | Synthesis of novel N-benzyl substituted piperidine amides of 1H-indole-5-carboxylic acid as potential inhibitors of cholinesterases | Acta poloniae pharmaceutica |
22425563 | 20120415 | Prospective acetylcholinesterase inhibitory activity of indole and its analogs | Bioorganic & medicinal chemistry letters |
21873044 | 20111115 | Immobilization of rat brain acetylcholinesterase on ZnS and poly(indole-5-carboxylic acid) modified Au electrode for detection of organophosphorus insecticides | Biosensors & bioelectronics |
20859573 | 20101101 | A label-free genosensor for BRCA1 related sequence based on impedance spectroscopy | The Analyst |
Complexity: | 193 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 161.047678466 |
Formal Charge: | 0 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 161.047678466 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 53.1 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.5 |
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