1427325-49-2
Catalog No.:AA009BKS

1427325-49-2 | JWH 018 6-methoxyindole analog

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥98%
in stock  
$116.00   $81.00
- +
5mg
≥98%
in stock  
$509.00   $356.00
- +
10mg
≥98%
in stock  
$903.00   $632.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA009BKS
Chemical Name:
JWH 018 6-methoxyindole analog
CAS Number:
1427325-49-2
Molecular Formula:
C25H25NO2
Molecular Weight:
371.4715
SMILES:
CCCCCn1cc(c2c1cc(OC)cc2)C(=O)c1cccc2c1cccc2
Properties
Computed Properties
 
Complexity:
521  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
7  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
6.3  

Literature
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Additional Info:
SDS
Tags:1427325-49-2 Molecular Formula|1427325-49-2 MDL|1427325-49-2 SMILES|1427325-49-2 JWH 018 6-methoxyindole analog
Catalog No.: AA009BKS
1427325-49-2
1427325-49-2 | JWH 018 6-methoxyindole analog
Pack Size: 1mg
Purity: ≥98%
in stock
$116.00 $81.00
Pack Size: 5mg
Purity: ≥98%
in stock
$509.00 $356.00
Pack Size: 10mg
Purity: ≥98%
in stock
$903.00 $632.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA009BKS
Chemical Name: JWH 018 6-methoxyindole analog
CAS Number: 1427325-49-2
Molecular Formula: C25H25NO2
Molecular Weight: 371.4715
SMILES: CCCCCn1cc(c2c1cc(OC)cc2)C(=O)c1cccc2c1cccc2
Properties
Complexity: 521  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 7  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 6.3  
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