CAS RN: 159-68-2
9,9′-Spirobi[9H-9-silafluorene]
Product Availability
Choose a grade to view its available package options.
1 package records 1 with current stock 1 grade group
Grade
98% (1)
In stock only
Batch No. Package Availability Warehouse Lead Time Inquiry
Batchno.20260426
250mg / 1g / 5g
Confirm by inquiry
Shanghai 5-7 business days Inquiry
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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: 1g
Available purity: >97%
Inventory rows with stock: 0
Bulk packaging: confirmed by inquiry
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Recorded sizes, purity and stock details for CAS 159-68-2
Pack Size
Recorded Purity
Available Qty
Ship From
Inquiry
1g
>97%
0
Out of Stock
Shenzhen
Inquiry
159-68-2 / 5,5'-spirobi[benzo[b][1]benzosilole]
Standard CAS: 159-68-2
Multi CAS: No
Basic Information
copy
CAS
159-68-2 copy
Multi CAS
No copy
Molecular Formula
C24H16Si copy
Molecular Weight
332.500000 copy
Exact Mass
332.102127 copy
SMILES
C1=CC=C2C(=C1)C3=CC=CC=C3[Si]24C5=CC=CC=C5C6=CC=CC=C46 copy
InChI
InChI=1S/C24H16Si/c1-5-13-21-17(9-1)18-10-2-6-14-22(18)25(21)23-15-7-3-11-19(23)20-12-4-8-16-24(20)25/h1-16H copy
InChIKey
FAMRBROKCVCCCX-UHFFFAOYSA-N copy
Computed Properties
copy
Structural Parameters
Heavy atom count
25 copy
Aromatic heavy atom count
24 copy
Molar refractivity
108.05 copy
TPSA
0.0000 copy
LogP / Solubility
WLOGP
3.02 copy
MLOGP
2.68 copy
XLogP3
3.02 copy
Consensus LogP
2.91 copy
Log S (ESOL)
-4.52 copy
Class (ESOL)
Slightly soluble copy
Log S (Ali)
-4.47 copy
Class (Ali)
Slightly soluble copy
Log S (SILICOS-IT)
-4.33 copy
Class (SILICOS-IT)
Slightly soluble copy
ADME
GI absorption
High copy
BBB permeant
Yes copy
P-gp substrate
No copy
CYP1A2 inhibitor
Yes copy
CYP2C19 inhibitor
Yes copy
CYP2C9 inhibitor
Yes copy
CYP2D6 inhibitor
No copy
CYP3A4 inhibitor
No copy
Log Kp (skin permeation)
-2.6 copy
Drug-likeness / Medicinal Chemistry
Lipinski
Yes copy
Ghose
Yes copy
Veber
Yes copy
Egan
Yes copy
Muegge
No copy
Bioavailability score
0.55 copy
Brenk alerts
1 copy
Leadlikeness
Yes copy
Synthetic Accessibility
5 copy