185424-57-1
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Basic information
- Product Name: 1H-Indol-6-amine, 3-(chloromethyl)-2,3-dihydro-N,N-dimethyl-1-[(5,6,7-trimethoxy-1H-indol -2-yl)carbonyl]-
- Synonyms:
- CAS NO:185424-57-1
- Molecular Formula: C23H26ClN3O4
- Molecular Weight:
- EINECS: N/A
- Product Categories: N/A
- Mol File: 185424-57-1.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1H-Indol-6-amine, 3-(chloromethyl)-2,3-dihydro-N,N-dimethyl-1-[(5,6,7-trimethoxy-1H-indol -2-yl)carbonyl]-(CAS DataBase Reference)
- NIST Chemistry Reference: 1H-Indol-6-amine, 3-(chloromethyl)-2,3-dihydro-N,N-dimethyl-1-[(5,6,7-trimethoxy-1H-indol -2-yl)carbonyl]-(185424-57-1)
- EPA Substance Registry System: 1H-Indol-6-amine, 3-(chloromethyl)-2,3-dihydro-N,N-dimethyl-1-[(5,6,7-trimethoxy-1H-indol -2-yl)carbonyl]-(185424-57-1)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 185424-57-1(Hazardous Substances Data)
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185424-57-1 Usage
Molecular Weight
394.84 g/molThe mass of one mole of the compound, based on the atomic weights of its constituent elements.
3. Indol-6-amine Core Structure
A bicyclic aromatic core consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring.
4. Chloromethyl Substituent (3-position)
A chlorine atom bonded to a methyl group (CH3) attached to the indole core at the third position, which can be useful for further functionalization and drug development.
5. N,N-Dimethyl Groups
Two methyl groups (CH3) attached to the nitrogen atom in the indole core, which can influence the compound's solubility, lipophilicity, and biological activity.
6. Carbonyl Group (1-position)
An oxygen double-bonded to a carbon atom (C=O) at the first position of the indole core, which can be important for the compound's reactivity and potential applications in organic synthesis.
7. Trimethoxyindolyl Moiety
A 5,6,7-trimethoxy substitution on the indole ring, consisting of three methoxy groups (OCH3) that can influence the compound's electronic properties and solubility.
Building block for drug development
The combination of functional groups in the compound makes it a promising candidate for the synthesis of pharmaceuticals.Organic synthesis
The presence of reactive functional groups, such as the carbonyl and chloromethyl groups, allows for further chemical reactions and modifications.Material science
The unique structure and properties of the compound may lead to applications in the development of new materials.Medicinal chemistry
The indol-6-amine core and other functional groups suggest potential biological activity, making it an interesting target for further study and drug discovery.Check Digit Verification of cas no
The CAS Registry Mumber 185424-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,4,2 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.Calculate Digit Verification of CAS Registry Number 185424-57:
(8*1)+(7*8)+(6*5)+(5*4)+(4*2)+(3*4)+(2*5)+(1*7)=151
151 % 10 = 1
So 185424-57-1 is a valid CAS Registry Number.
185424-57-1Upstream product
185424-57-1Downstream Products
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1H-Indol-6-amine,
3-(chloromethyl)-2,3-dihydro-N,N-dimethyl-1-[(5,6,7-trimethoxy-1H-indol
-2-yl)carbonyl]-
