CAS RN: 162401-16-3
2-Furan-2-yl-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyriMidin-5-ylaMine
Product Availability
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2 package records0 with current stock1 grade group
| Batch No. | Package | Availability | Inquiry |
| Batchno.20260310 |
100mg |
Out of stock |
Inquiry |
| Batchno.20250223 |
250mg |
Out of stock |
Inquiry |
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Packaging options, recorded purity, stock quantity and ship-from location below are generated from the current factory data table for this CAS.
- Pack sizes on record: 0.1g, 0.25g, 1g
- Available purity: ≥95%
- Inventory rows with stock: 2
- Bulk packaging: confirmed by inquiry
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Recorded sizes, purity and stock details for CAS 162401-16-3
| Pack Size |
Recorded Purity |
Available Qty |
Ship From |
Inquiry |
| 0.1g |
≥95% |
1
In Stock
|
Shenzhen |
Inquiry |
| 0.25g |
≥95% |
1
In Stock
|
Shanghai |
Inquiry |
| 1g |
≥95% |
0
Out of Stock
|
Hong Kong |
Inquiry |
162401-16-3 / 4-(furan-2-yl)-3,5,6,8,10,11-hexazatricyclo[7.3.0.02,6]dodeca-1(9),2,4,7,11-pentaen-7-amine
Standard CAS: 162401-16-3
Multi CAS: No
Basic Information
CAS
162401-16-3
Multi CAS
No
Molecular Formula
C10H7N7O
Molecular Weight
241.210000
Exact Mass
241.071208
SMILES
C1=COC(=C1)C2=NN3C(=N2)C4=C(NN=C4)N=C3N
InChI
InChI=1S/C10H7N7O/c11-10-14-7-5(4-12-15-7)9-13-8(16-17(9)10)6-2-1-3-18-6/h1-4H,(H3,11,12,14,15)
InChIKey
YKWJNVFPKLFRRE-UHFFFAOYSA-N
Computed Properties
Structural Parameters
Heavy atom count
18
Aromatic heavy atom count
17
Rotatable bonds
1
H-bond acceptors
7
H-bond donors
2
Molar refractivity
62.55
TPSA
110.92
LogP / Solubility
WLOGP
0.84
MLOGP
0.75
XLogP3
0.5
Consensus LogP
0.7
Log S (ESOL)
-2.5
Class (ESOL)
Moderately soluble
Log S (Ali)
-2.15
Class (Ali)
Moderately soluble
Log S (SILICOS-IT)
-2.05
Class (SILICOS-IT)
Moderately soluble
ADME
GI absorption
High
BBB permeant
No
P-gp substrate
No
CYP1A2 inhibitor
No
CYP2C19 inhibitor
No
CYP2C9 inhibitor
No
CYP2D6 inhibitor
No
CYP3A4 inhibitor
No
Log Kp (skin permeation)
-3.59
Drug-likeness / Medicinal Chemistry
Lipinski
Yes
Ghose
No
Veber
Yes
Egan
Yes
Muegge
Yes
Bioavailability score
0.55
Leadlikeness
No
Synthetic Accessibility
2