56915
Indazole-3-carboxylic acid
≥97.0% (HPLC)
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About This Item
Empirical Formula (Hill Notation):
C8H6N2O2
CAS Number:
Molecular Weight:
162.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-794-5
Beilstein/REAXYS Number:
6354
MDL number:
Assay:
≥97.0% (HPLC)
Form:
powder
assay
≥97.0% (HPLC)
form
powder
color
beige
mp
266-270 °C (dec.)
SMILES string
OC(=O)c1n[nH]c2ccccc12
InChI
1S/C8H6N2O2/c11-8(12)7-5-3-1-2-4-6(5)9-10-7/h1-4H,(H,9,10)(H,11,12)
InChI key
BHXVYTQDWMQVBI-UHFFFAOYSA-N
Application
Indazole-3-carboxylic acid may be used in the synthesis of the following:
- N-(8-methyl-azabicyclo[3.2.11]oct-3-yl)-1H-indazole-3-carboxamide
- N-(1- benzyl-4-methylhexahydro-1H-1,4-diazepin-6-yl)-1H-indazole-3-carboxamide
- 1H-indazole-3-carboxamide
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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P Khanna et al.
Biochemistry, 40(5), 1441-1450 (2001-02-15)
N-Methyltryptophan oxidase (MTOX) is a flavoenzyme that catalyzes the oxidative demethylation of N-methyl-L-tryptophan and other N-methyl amino acids, including sarcosine, which is a poor substrate. The Escherichia coli gene encoding MTOX (solA) was isolated on the basis of its sequence
Basic and applied research in the study of indazole carboxylic acids.
B Silvestrini
Chemotherapy, 27 Suppl 2, 9-20 (1981-01-01)
Per Ole M Gundersen et al.
Drug testing and analysis, 11(1), 51-67 (2018-07-12)
Synthetic cannabinoids are one of the most significant groups within the category new psychoactive substances (NPS) and in recent years new compounds have continuously been introduced to the market of recreational drugs. A sensitive and quantitative screening method in urine
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 56915-10G | 04061832597058 |
| 56915-50G | 04061833448915 |