2-Nitrobenzaldehyde, 98%

Name: 2-Nitrobenzaldehyde, 98% | 552-89-6
Brand: J&K Chemical
SKU: JK225302_500_G
Price: 543.0 USD
Availability: OutOfStock

Cat. No JK225302_500_G

Vendor: J&K Chemical

Product Information

Product Name

2-Nitrobenzaldehyde, 98%

Brand Name

J&K

Product Number

225302

CAS

552-89-6

Molecular Formula

C7H5NO3

Molecular Weight

151.12

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11101

IUPAC Name

2-nitrobenzaldehyde

InChI Key

CMWKITSNTDAEDT-UHFFFAOYSA-N

SMILES

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

Properties

Melting Point

42-44

Boiling Point

153

Flash Point

113

Safety Information

Signal Word

Warning

Hazard Statement

H302

H315

H319

H335

Precautionary Statement

P270

P330

P501

P280

P321

P261

P271

P319

P405

P301+P317

P302+P352

P332+P317

P362+P364

P264+P265

P305+P351+P338

P337+P317

P304+P340

P403+P233

References Data Source From Pubchem

Material to synthetic efficiency: Novel AMP modified g-C3N4·SO3H catalyst for the green and scalable synthesis of xanthene-1,8-diones

Publication Name: Research on Chemical Intermediates

Publication Date: 2026-02-26

DOI: 10.1007/s11164-026-05952-x

Exploring MAO inhibitory activity of 5-hydroxy regioisomers of hispidol’s analogs leads to identification of novel highly selective MAO-B open-conformation inhibitors

Publication Name: Molecular Diversity

Publication Date: 2026-02-01

DOI: 10.1007/s11030-025-11464-4

Targeting Alzheimer’s diseases via nitro-substituted Schiff base derivatives: synthesis, DFT, and molecular dynamics studies

Publication Name: In Silico Pharmacology

Publication Date: 2026-01-14

DOI: 10.1007/s40203-025-00544-w

Electrocatalytic Hydrogen Evolution Reaction of A2B-Type Triaryl Corrole Copper Complexes

Publication Name: Catalysis Letters

Publication Date: 2026-01-03

DOI: 10.1007/s10562-025-05285-1

Thermomicroscopy–calorimetry applied to chemical and biological systems

Publication Name: Journal of Thermal Analysis and Calorimetry

Publication Date: 2025-12

DOI: 10.1007/s10973-025-15180-x

2-Nitrobenzaldehyde, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Material to synthetic efficiency: Novel AMP modified g-C3N4·SO3H catalyst for the green and scalable synthesis of xanthene-1,8-diones

Exploring MAO inhibitory activity of 5-hydroxy regioisomers of hispidol’s analogs leads to identification of novel highly selective MAO-B open-conformation inhibitors

Targeting Alzheimer’s diseases via nitro-substituted Schiff base derivatives: synthesis, DFT, and molecular dynamics studies

Electrocatalytic Hydrogen Evolution Reaction of A2B-Type Triaryl Corrole Copper Complexes

Thermomicroscopy–calorimetry applied to chemical and biological systems