3-Nitrobenzamide - ≥98%(GC) , CAS No.645-09-0

CAS: 645-09-0 Cat. No.: N159415 Formule: C7H6N2O3 Poids moléculaire: 166.14 Beilstein Registry Number: 9381 Numéro CE: 211-431-0
DISPONIBLE À COMMANDE
GRADE & PURITY ≥98%(GC)
Synonyms
SY076647 | NITROBENZAMIDE, M- | AE-562/40173655 | AKOS000283200 | EN300-49218 | AC-10271 | 3-nitrophenylcarboxamide | MLS002415746 | NCGC00091263-01 | UNII-KMU7X7KT5T | AS-19826 | NSC37327 | NSC-37327 | J-512967 | NCGC00091263-02 | NSC 37327 | Tox21_20009
Storage
Room temperature
Shipped In
Normal
★
Size
Allemagne (EU)
USA*
Price
Qty
1g
N159415-1g
Sur commande · 8–12 semaines

8,59€

12,93€
Enregistrer 4,34 € (33.56%)
5g
N159415-5g
—
En stock ≥10

13,80€

20,74€
Enregistrer 6,94 € (33.47%)
25g
N159415-25g
—
1 En stock

23,34€

35,49€
Enregistrer 12,15 € (34.23%)
100g
N159415-100g
—
1 En stock

92,76€

139,62€
Enregistrer 46,86 € (33.56%)
500g
N159415-500g
Sur commande · 8–12 semaines

347,88€

522,29€
Enregistrer 174,42 € (33.39%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥98%(GC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonymes
SY076647 | NITROBENZAMIDE, M- | AE-562/40173655 | AKOS000283200 | EN300-49218 | AC-10271 | 3-nitrophenylcarboxamide | MLS002415746 | NCGC00091263-01 | UNII-KMU7X7KT5T | AS-19826 | NSC37327 | NSC-37327 | J-512967 | NCGC00091263-02 | NSC 37327 | Tox21_20009
Spécifications et pureté
≥98%(GC)
Conditions de stockage de stockage
Room temperature
Expédié en
Normal
Pureté
≥98%(GC)
Noms et identifiants
Pubchem Sid488181704
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488181704
Sourires canoniquesC1=CC(=CC(=C1)[N+](=O)[O-])C(=O)N
IUPAC Name3-nitrobenzamide
InChIKeyKWAYEPXDGHYGRW-UHFFFAOYSA-N
INCHI1S/C7H6N2O3/c8-7(10)5-2-1-3-6(4-5)9(11)12/h1-4H,(H2,8,10)
Isomères SMILES C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)N
WGK Allemagne 3
RTECS CV5601250
Poids moléculaire 166.14
Beilstein 9381
Reaxy-Rn 777185
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=777185&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassNitrobenzenes
Intermediate Tree Nodes Not available
Direct ParentNitrobenzenes
Alternative Parents Benzamides  Nitroaromatic compounds  Benzoyl derivatives  Primary carboxylic acid amides  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Benzamide - Benzoic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Benzoyl - Carboxamide group - C-nitro compound - Primary carboxylic acid amide - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic zwitterion - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as nitrobenzenes. These are compounds containing a nitrobenzene moiety, which consists of a benzene ring with a carbon bearing a nitro group.
External Descriptors Not available
Structure 3D
Modèle de structure chimique interactif





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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

3 results found

Lot NumberCertificate TypeDateArticle
D2020144Certificate of AnalysisFeb 23, 2024 N159415
L2312060Certificate of AnalysisDec 14, 2023 N159415
D2323790Certificate of AnalysisMay 05, 2023 N159415
Propriétés chimiques et physiques
Point de fusion (°C)143-146°C
Poids moléculaire166.130 g/mol
XLogP30.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass166.038 Da
Monoisotopic Mass166.038 Da
Topological Polar Surface Area88.900 Ų
Heavy Atom Count12
Formal Charge0
Complexity199.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Références
1. Xuan Gao, Min Cao, Xudong Qi, Dongsheng Zhang, Zhihui Li, Xinqiang Zhao, Yanji Wang.  (2026)  One-step liquid-phase ammonia oxidation of 5-hydroxymethylfurfural to 5-hydroxymethylfurfurylamide.  CHEMICAL ENGINEERING SCIENCE,      [PMID:] [10.1016/j.ces.2026.123591]
Calculateurs de solution
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