CAS RN: 721960-43-6
4-Amino-3-chlorophenylboronic acid, pinacol ester
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Choose a grade to view its available package options.
3 package records3 with current stock1 grade group
| Batch No. | Package | Availability | Inquiry |
| Batchno.20251110 |
1g |
In stock |
Inquiry |
| Batchno.20260202 |
250mg |
In stock |
Inquiry |
| Batchno.20250309 |
5g |
In 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: 0.25g, 1g, 5g
- Available purity: >97%
- Inventory rows with stock: 1
- Bulk packaging: confirmed by inquiry
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Recorded sizes, purity and stock details for CAS 721960-43-6
| Pack Size |
Recorded Purity |
Available Qty |
Ship From |
Inquiry |
| 0.25g |
>97% |
1
In Stock
|
Shenzhen |
Inquiry |
| 1g |
>97% |
0
Out of Stock
|
Shanghai |
Inquiry |
| 5g |
>97% |
0
Out of Stock
|
Shenzhen |
Inquiry |
721960-43-6 / 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
Standard CAS: 721960-43-6
Multi CAS: Yes
Basic Information
CAS
721960-43-6
Multi CAS
Yes
Molecular Formula
C12H17BCLNO2
Molecular Weight
253.530000
Exact Mass
253.104087
InChI
InChI=1S/C12H17BClNO2/c1-11(2)12(3,4)17-13(16-11)8-5-6-10(15)9(14)7-8/h5-7H,15H2,1-4H3
InChIKey
BEXOYZKPTUJSCZ-UHFFFAOYSA-N
Computed Properties
Structural Parameters
Heavy atom count
17
Aromatic heavy atom count
6
Fraction Csp3
0.5
Rotatable bonds
1
H-bond acceptors
3
H-bond donors
1
Molar refractivity
71.58
TPSA
44.48
LogP / Solubility
WLOGP
2.22
MLOGP
1.96
XLogP3
2.22
Consensus LogP
2.13
Log S (ESOL)
-3.01
Class (ESOL)
Poorly soluble
Log S (Ali)
-3.24
Class (Ali)
Poorly soluble
Log S (SILICOS-IT)
-3.27
Class (SILICOS-IT)
Poorly soluble
ADME
GI absorption
High
BBB permeant
Yes
P-gp substrate
No
CYP1A2 inhibitor
No
CYP2C19 inhibitor
No
CYP2C9 inhibitor
No
CYP2D6 inhibitor
Yes
CYP3A4 inhibitor
No
Log Kp (skin permeation)
-2.69
Drug-likeness / Medicinal Chemistry
Lipinski
Yes
Ghose
No
Veber
Yes
Egan
Yes
Muegge
Yes
Bioavailability score
0.55
Brenk alerts
1
Leadlikeness
Yes
Synthetic Accessibility
1.5