CAS RN: 1356412-82-2
5-broMo-2-nitroisonicotinic acid
Product Availability
Choose a grade to view its available package options.
1 package records 0 with current stock 1 grade group
Grade
98% (1)
In stock only
Batch No. Package Availability Lead Time Inquiry
Batchno.20250817
50mg
Out of stock
8-10 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 1356412-82-2
Pack Size
Recorded Purity
Available Qty
Ship From
Inquiry
1g
>97%
0
Out of Stock
Beijing
Inquiry
1356412-82-2 / 5-bromo-2-nitropyridine-4-carboxylic acid
Standard CAS: 1356412-82-2
Multi CAS: No
Basic Information
copy
CAS
1356412-82-2 copy
Multi CAS
No copy
Molecular Formula
C6H3BrN2O4 copy
Molecular Weight
247.000000 copy
Exact Mass
245.927620 copy
SMILES
C1=C(C(=CN=C1[N+](=O)[O-])Br)C(=O)O copy
InChI
InChI=1S/C6H3BrN2O4/c7-4-2-8-5(9(12)13)1-3(4)6(10)11/h1-2H,(H,10,11) copy
InChIKey
MPPXDSQZQIBCRT-UHFFFAOYSA-N copy
Computed Properties
copy
Structural Parameters
Heavy atom count
13 copy
Aromatic heavy atom count
6 copy
Rotatable bonds
2 copy
H-bond acceptors
4 copy
H-bond donors
1 copy
Molar refractivity
45.55 copy
TPSA
93.33 copy
LogP / Solubility
WLOGP
1.45 copy
MLOGP
1.28 copy
XLogP3
1.2 copy
Consensus LogP
1.31 copy
Log S (ESOL)
-2.49 copy
Class (ESOL)
Moderately soluble copy
Log S (Ali)
-2.63 copy
Class (Ali)
Moderately soluble copy
Log S (SILICOS-IT)
-2.71 copy
Class (SILICOS-IT)
Moderately soluble copy
ADME
GI absorption
High copy
BBB permeant
No copy
P-gp substrate
No copy
CYP1A2 inhibitor
No copy
CYP2C19 inhibitor
No copy
CYP2C9 inhibitor
No copy
CYP2D6 inhibitor
No copy
CYP3A4 inhibitor
No copy
Log Kp (skin permeation)
-3.2 copy
Drug-likeness / Medicinal Chemistry
Lipinski
Yes copy
Ghose
No copy
Veber
Yes copy
Egan
Yes copy
Muegge
Yes copy
Bioavailability score
0.55 copy
Brenk alerts
1 copy
Leadlikeness
No copy
Synthetic Accessibility
1.5 copy