4-Bromo-3-nitro-benzoic acid, 98%

Name: 4-Bromo-3-nitro-benzoic acid, 98% | 6319-40-0
Brand: J&K Chemical
SKU: JK969107_5_G
Price: 68.5 USD
Availability: InStock

Cat. No JK969107_5_G

Vendor: J&K Chemical

Product Information

Product Name

4-Bromo-3-nitro-benzoic acid, 98%

Brand Name

J&K

Product Number

969107

CAS

6319-40-0

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

232986

IUPAC Name

4-bromo-3-nitrobenzoic acid

InChI Key

RVCTZJVBWNFYRU-UHFFFAOYSA-N

SMILES

C1=CC(=C(C=C1C(=O)O)N+(=O)O-)Br

Safety Information

Storage Condition

Store at 2-8℃

References

Reorganized, weak C–H⋯O interactions directly modify the mechanical properties and compaction performance of a series of nitrobenzoic acids

Publication Name: CrystEngComm

Publication Date: 2017

DOI: 10.1039/c7ce00238f

Solid-Supported Synthesis of Indoles via Gold-Catalyzed Cyclization

Publication Name: Synfacts

Publication Date: 2012-05-16

DOI: 10.1055/s-0031-1291028

From 2-(o-Aminoaryl)acetaldehyde Acetals or Hemiacetals

Publication Name: Science of Synthesis

Publication Date: 2010

From 2-(o-Aminoaryl)acetaldehyde Acetals or Hemiacetals

Publication Name: Science of Synthesis

Publication Date: 2001

C21Co - C21H24 (3912 - 3971)

Publication Name: Landolt-Börnstein - Group III Condensed Matter

Publication Date: 1985

DOI: 10.1007/10201616_19

4-Bromo-3-nitro-benzoic acid, 98%

Product Information

General Information

Safety Information

References

Reorganized, weak C–H⋯O interactions directly modify the mechanical properties and compaction performance of a series of nitrobenzoic acids

Solid-Supported Synthesis of Indoles via Gold-Catalyzed Cyclization

From 2-(o-Aminoaryl)acetaldehyde Acetals or Hemiacetals

From 2-(o-Aminoaryl)acetaldehyde Acetals or Hemiacetals

C21Co - C21H24 (3912 - 3971)