CAS RN: 1402709-93-6
3H-IMidazo[4,5-b]pyridine, 6-chloro-7-[4-[(4-chlorophenyl)Methyl]-1-piperazinyl]-2-(1,3-diMethyl-1H-pyrazol-4-yl)-
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This product has historical factory records. Recorded pack sizes and purity can be used as a supply reference, while project-specific availability is confirmed by inquiry.
Pack sizes on record: 0.25g
Available purity: ≥95%
Inventory rows with stock: 0
Bulk packaging: confirmed by inquiry
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Recorded sizes, purity and stock details for CAS 1402709-93-6
Pack Size
Recorded Purity
Available Qty
Ship From
Inquiry
0.25g
≥95%
0
Out of Stock
Shenzhen
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1402709-93-6 / 6-chloro-7-[4-[(4-chlorophenyl)methyl]piperazin-1-yl]-2-(1,3-dimethylpyrazol-4-yl)-1H-imidazo[4,5-b]pyridine
Standard CAS: 1402709-93-6
Multi CAS: No
Basic Information
copy
CAS
1402709-93-6 copy
Multi CAS
No copy
Molecular Formula
C22H23Cl2N7 copy
Molecular Weight
456.400000 copy
Exact Mass
455.139199 copy
SMILES
CC1=NN(C=C1C2=NC3=NC=C(C(=C3N2)N4CCN(CC4)CC5=CC=C(C=C5)Cl)Cl)C copy
InChI
InChI=1S/C22H23Cl2N7/c1-14-17(13-29(2)28-14)21-26-19-20(18(24)11-25-22(19)27-21)31-9-7-30(8-10-31)12-15-3-5-16(23)6-4-15/h3-6,11,13H,7-10,12H2,1-2H3,(H,25,26,27) copy
InChIKey
AKJBLKUZXRMECW-UHFFFAOYSA-N copy
Computed Properties
copy
Structural Parameters
Heavy atom count
31 copy
Aromatic heavy atom count
20 copy
Fraction Csp3
0.32 copy
Rotatable bonds
4 copy
H-bond acceptors
6 copy
H-bond donors
1 copy
Molar refractivity
124.78 copy
TPSA
65.87 copy
LogP / Solubility
WLOGP
4.3 copy
MLOGP
3.81 copy
XLogP3
3.8 copy
Consensus LogP
3.97 copy
Log S (ESOL)
-5.59 copy
Class (ESOL)
Slightly soluble copy
Log S (Ali)
-6.4 copy
Class (Ali)
Insoluble copy
Log S (SILICOS-IT)
-6.67 copy
Class (SILICOS-IT)
Insoluble copy
ADME
GI absorption
High copy
BBB permeant
No copy
P-gp substrate
No copy
CYP1A2 inhibitor
Yes copy
CYP2C19 inhibitor
Yes copy
CYP2C9 inhibitor
Yes copy
CYP2D6 inhibitor
Yes copy
CYP3A4 inhibitor
Yes copy
Log Kp (skin permeation)
-2.45 copy
Drug-likeness / Medicinal Chemistry
Lipinski
Yes copy
Ghose
Yes copy
Veber
Yes copy
Egan
Yes copy
Muegge
Yes copy
Bioavailability score
0.55 copy
Leadlikeness
No copy
Synthetic Accessibility
3.5 copy