Catalogue Number
BN-O1166
Analysis Method
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
133.15
Appearance
Botanical Source
Structure Type
Category
SMILES
C1=CC2=C(C=C1N)C=NN2
Synonyms
IFLAB-BB F2108-0020/5-AMINOINDAZOLE/5-amino-1h-indazol/5-amino-1h-indazole/5-Amino (1H)indazole/indazol-5-ylamine/1H-indazol-5-yl amine/1H-Indazol-6-amine/1H-Indazol-5-amine/6-Amino-1H-indazole/1H-Indazole-5-amine/2H-Indazol-6-amine/5-indazolamine/5-Amino(1H)indazole
IUPAC Name
1H-indazol-5-amine
Density
1.4±0.1 g/cm3
Solubility
Flash Point
209.5±7.6 °C
Boiling Point
376.6±15.0 °C at 760 mmHg
Melting Point
175-178 °C(lit.)
InChl
InChl Key
XBTOSRUBOXQWBO-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:19335-11-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
20814822
Six new series of pyrazolo[4,3-f]quinoline derivatives with potential bioactivities were synthesized by the three-component reactions of aromatic aldehydes, 5-aminoindazole, and various cyclic 1,3-dicarbonyl compounds under microwave irradiation. This protocol has the valuable features of structural diversity of products, broader substrate scope, operational simplicity, high yields, and short reaction time. Moreover, the structure of compound 88a was confirmed by an X-ray crystallographic analysis and attested to the chemoselectivity of reaction where 1-methyl barbituric acid participated.
A Diversity-Oriented Synthesis of pyrazolo[4,3-f]quinoline Derivatives With Potential Bioactivities via Microwave-Assisted Multi-Component Reactions
Feng Shi 1, Shu Zhang, Shan-Shan Wu, Yuan Gao, Shu-Jiang Tu
2011 May
21078554
Affinity reagents that target protein kinases are powerful tools for signal transduction research. Here, we describe a general set of kinase ligands based on a 5-aminoindazole scaffold. This scaffold can readily be derivatized with diverse binding elements and immobilized analogs allow selective enrichment of protein kinases from complex mixtures.
Protein Kinase Affinity Reagents Based on a 5-aminoindazole Scaffold
Ratika Krishnamurty 1, Amanda M Brock, Dustin J Maly
2011 Jan 1
16827557
A microwave-assisted parallel synthesis of 2,4-disubstituted 5-aminoimidazoles has been developed. Significant rate enhancement was observed for all steps in the three-step protocol. The overall reaction time was shortened to 25 min, as compared to 53 h for the conventional procedures. A representative set of 2,4-disubstituted 5-aminoimidazoles was prepared using commercially available parallel reactors.
Synthesis of 2,4-disubstituted 5-aminoimidazoles Using Microwave Irradiation
Chai Hoon Soh 1, Wai Keung Chui, Yulin Lam
Jul-Aug 2006