4-Acetamido-3-Nitroanisole - ≥95% , CAS No.119-81-3

CAS: 119-81-3 Cat. No.: A166380 Fórmula: C9H10N2O4 Peso molecular: 210.191 Número CE: 204-353-3
Disponível para encomenda
GRADE & PURITY ≥95%
Synonyms
4-Acetamido-3-nitroanisole | N-(4-Methoxy-2-nitrophenyl)acetamide | N-(4-methoxy-2-nitro-phenyl)acetamide | N-(4-methoxy-2-nitro-phenyl)-acetamide | AF-966/00544054 | HMS559L21 | NSC5516 | NSC-5516 | A804363 | 4-Methoxy-2-nitro acetanilide | AKOS015996800
Storage
Room temperature
Shipped In
Normal
★
Size
Alemanha (EU)
USA*
Price
Qty
1g
A166380-1g
—
5 Em stock
19,87€
5g
A166380-5g
—
8 Em stock
43,30€
25g
A166380-25g
—
5 Em stock
161,31€
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% 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

Sinónimos
4-Acetamido-3-nitroanisole | N-(4-Methoxy-2-nitrophenyl)acetamide | N-(4-methoxy-2-nitro-phenyl)acetamide | N-(4-methoxy-2-nitro-phenyl)-acetamide | AF-966/00544054 | HMS559L21 | NSC5516 | NSC-5516 | A804363 | 4-Methoxy-2-nitro acetanilide | AKOS015996800
Especificações e pureza
≥95%
Condições de armazenamento de armazenamento
Room temperature
Enviado em
Normal
Pureza
≥95%
Nomes e identificadores
Pubchem Sid504754115
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504754115
Sorrisos canónicosCC(=O)NC1=C(C=C(C=C1)OC)[N+](=O)[O-]
IUPAC NameN-(4-methoxy-2-nitrophenyl)acetamide
InChIKeyQGEGALJODPBPGR-UHFFFAOYSA-N
INCHI1S/C9H10N2O4/c1-6(12)10-8-4-3-7(15-2)5-9(8)11(13)14/h3-5H,1-2H3,(H,10,12)
SMILES isoméricas CC(=O)NC1=C(C=C(C=C1)OC)[N+](=O)[O-]
Peso molecular 210.191
Reaxy-Rn 2809678
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2809678&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 ParentNitrophenyl ethers
Alternative Parents Acetanilides  N-acetylarylamines  Methoxyanilines  Phenoxy compounds  Nitroaromatic compounds  Methoxybenzenes  Anisoles  Alkyl aryl ethers  Acetamides  Secondary carboxylic acid amides  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Carbonyl compounds  Hydrocarbon derivatives  Organic oxides  Organic zwitterions  Organopnictogen compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Nitrophenyl ether - Acetanilide - Anilide - Methoxyaniline - N-acetylarylamine - Anisole - Phenol ether - Methoxybenzene - N-arylamide - Nitroaromatic compound - Phenoxy compound - Alkyl aryl ether - Acetamide - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Carboxylic acid derivative - Ether - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organopnictogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Organic zwitterion - Aromatic homomonocyclic compound
DescriçãoThis compound belongs to the class of organic compounds known as nitrophenyl ethers. These are aromatic compounds containing a nitrobenzene moiety that carries an ether group on the benzene ring.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

5 results found

Lot NumberCertificate TypeDataItem
J2213033Certificate of AnalysisJul 06, 2026 A166380
J2213034Certificate of AnalysisJul 06, 2026 A166380
J1928064Certificate of AnalysisAug 04, 2023 A166380
E2320389Certificate of AnalysisJul 26, 2022 A166380
E2320394Certificate of AnalysisJul 26, 2022 A166380
Propriedades químicas e físicas
Ponto de fusão (°C)117-118℃
Peso molecular210.190 g/mol
XLogP31.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass210.064 Da
Monoisotopic Mass210.064 Da
Topological Polar Surface Area84.200 Ų
Heavy Atom Count15
Formal Charge0
Complexity251.000
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
Referências
1. Zhiquan An, Siying Chen, Tao Lu, Pengjun Zhao, Xiaodong Yang, Yang Li, Juan Hou.  (2023)  Interfacial modification via aniline molecules with multiple active sites for performance enhancement of n–i–p perovskite solar cells.  Journal of Materials Chemistry C,  11  (37): (12750-12758).  [PMID:] [10.1039/D3TC02144K]
Calculadoras de soluções
Revisões

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