CAS RN: 932033-58-4
2,2′-Binaphthalene-6,6′-dicarboxylic Acid
Product Availability
Choose a grade to view its available package options.
7 package records7 with current stock2 grade groups
| Batch No. | Package | Availability | Warehouse | Lead Time | Inquiry |
|---|---|---|---|---|---|
| Batchno.20250119 | 100mg / 250mg / 1g / 5g | Confirm by inquiry | Shanghai | 8-10 business days | Inquiry |
| Batch No. | Package | Availability | Warehouse | Lead Time | Inquiry |
|---|---|---|---|---|---|
| Batchno.20260101 | 100mg | In stock | Shanghai, Tianjin, Wuhan, Chengdu | Inquiry | |
| Batchno.20250421 | 10g | In stock | Shanghai | Inquiry | |
| Batchno.20251206 | 1g | In stock | Shanghai, Shenzhen | Inquiry | |
| Batchno.20260114 | 250mg | In stock | Shanghai, Shenzhen, Wuhan | Inquiry | |
| Batchno.20250501 | 25g | In stock | Shanghai | Inquiry | |
| Batchno.20250816 | 5g | In stock | Shanghai | Inquiry |
- Product code: starshine_CAS932033-58-4
- Purity/Analytical Methods: >99.0%
932033-58-4 / 6-(6-carboxynaphthalen-2-yl)naphthalene-2-carboxylic acid
Basic Information
CAS
932033-58-4
Multi CAS
No
Molecular Formula
C22H14O4
Molecular Weight
342.300000
Exact Mass
342.089209
InChI
InChI=1S/C22H14O4/c23-21(24)19-7-5-15-9-13(1-3-17(15)11-19)14-2-4-18-12-20(22(25)26)8-6-16(18)10-14/h1-12H,(H,23,24)(H,25,26)
InChIKey
HWEIPTRZTZNYNO-UHFFFAOYSA-N
Computed Properties
Structural Parameters
Heavy atom count
26
Aromatic heavy atom count
20
Rotatable bonds
3
H-bond acceptors
2
H-bond donors
2
Molar refractivity
100.81
TPSA
74.6
LogP / Solubility
WLOGP
5.06
MLOGP
4.47
XLogP3
5.1
Consensus LogP
4.88
Log S (ESOL)
-5.52
Class (ESOL)
Slightly soluble
Log S (Ali)
-6.02
Class (Ali)
Insoluble
Log S (SILICOS-IT)
-6.44
Class (SILICOS-IT)
Insoluble
ADME
GI absorption
High
BBB permeant
No
P-gp substrate
No
CYP1A2 inhibitor
Yes
CYP2C19 inhibitor
Yes
CYP2C9 inhibitor
Yes
CYP2D6 inhibitor
No
CYP3A4 inhibitor
No
Log Kp (skin permeation)
-1.22
Drug-likeness / Medicinal Chemistry
Lipinski
Yes
Ghose
Yes
Veber
Yes
Egan
Yes
Muegge
No
Bioavailability score
0.55
Leadlikeness
No
Synthetic Accessibility
3
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