889674-99-1 Usage
Classification
Benzyl-substituted indole derivative, phenethylamine
Functional groups
Indole, benzyl, ethyl, and methyl groups
Physical state
Likely a solid (based on molecular size and complexity)
Appearance
Unknown, but may be a colorless or white solid
Solubility
Likely soluble in organic solvents such as ethanol, methanol, or acetone
Melting point
Unknown, but expected to be relatively high due to the molecular size and complexity
Boiling point
Unknown, but expected to be relatively high due to the molecular size and complexity
Density
Unknown, but likely to be higher than water due to the molecular size and complexity
Uses
Production of pharmaceutical drugs, synthesis of new compounds for medicinal and research purposes
Applications
Potential therapeutic applications, valuable building block for the development of new drugs
Stability
Unknown, but may be sensitive to light, heat, or moisture (common for organic compounds)
Reactivity
Unknown, but may react with strong acids, strong bases, or oxidizing agents (common for organic compounds)
Safety
Unknown, but should be handled with care due to its potential use in pharmaceuticals and research
Disposal
Should be disposed of according to local regulations and guidelines for hazardous chemicals
Environmental impact
Unknown, but may have potential environmental risks due to its use in pharmaceuticals and research
Synthesis
Likely synthesized through a multi-step process involving the formation of the indole core, followed by the introduction of the benzyl, ethyl, and methyl substituents, and finally the hydroxylation at the 4-position.
Check Digit Verification of cas no
The CAS Registry Mumber 889674-99-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,6,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 889674-99:
(8*8)+(7*8)+(6*9)+(5*6)+(4*7)+(3*4)+(2*9)+(1*9)=271
271 % 10 = 1
So 889674-99-1 is a valid CAS Registry Number.
889674-99-1Relevant academic research and scientific papers
The first potent inhibitor of mammalian group X secreted phospholipase A2: Elucidation of sites for enhanced binding
Smart, Brian P.,Oslund, Rob C.,Walsh, Laura A.,Gelb, Michael H.
, p. 2858 - 2860 (2007/10/03)
Using the X-ray structure of human group X secreted phospholipase A 2 (hGX), we carried out structure-based design of indole-based inhibitors and prepared the compounds using a new synthetic route. The most potent compound inhibited hGX and the mouse orthologue with an IC50 of 75 nM. This compound is the most potent hGX inhibitor reported to date and was also found to inhibit a subset of the other mouse and human SPLA 2S.
