4-Methoxybenzoic acid - Melting point standard, used for This product is an analytical standard and used for melting point calibration. various applications , CAS No.100-09-4

CAS: 100-09-4 Cat. No.: M119543 Fórmula: C₈H₈O₃ Peso molecular: 152.15 Beilstein Registry Number: 508910 Número CE: 202-818-5

GRADE & PURITY Melting point standard

Synonyms

4-METHOXYBENZOIC ACID | p-Anisic acid | p-Methoxybenzoic acid | Draconic acid

Storage

Room temperature

Shipped In

Normal

Visão geral

The melting point standard for p-anisic acid is 182-184℃, which can be used for the identification or purity determination of substances through conventional identification methods. Its melting point value is the average of 6 to 12 measurements obtained using a Büchi B-545 melting point apparatus, which has been calibrated using primary standard materials.

Features and Advantages: 

Melting point determined by thermodynamic analysis method 

Standard deviation up to ±0.3 °C

Specifications

Sinónimos

4-METHOXYBENZOIC ACID | p-Anisic acid | p-Methoxybenzoic acid | Draconic acid

Especificações e pureza

Melting point standard

Aplicação

This product is an analytical standard and used for melting point calibration.

Condições de armazenamento de armazenamento

Room temperature

Enviado em

Normal

Tipo de ação

INHIBITOR

Nomes e identificadores

Pubchem Sid

504751357

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504751357

Sorrisos canónicos

COC1=CC=C(C=C1)C(=O)O

IUPAC Name

4-methoxybenzoic acid

InChIKey

ZEYHEAKUIGZSGI-UHFFFAOYSA-N

INCHI

1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)

SMILES isoméricas

COC1=CC=C(C=C1)C(=O)O

WGK Alemanha

1

RTECS

BZ4395000

Peso molecular

152.15

Beilstein

508910

Reaxy-Rn

508910

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=508910&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Benzoic acids and derivatives
        • Level5 Methoxybenzoic acids and derivatives
          • Level6 P-methoxybenzoic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Benzoic acids and derivatives
• Intermediate Tree Nodes: Methoxybenzoic acids and derivatives
• Direct Parent: P-methoxybenzoic acids and derivatives
• Alternative Parents: Benzoic acids Phenoxy compounds Methoxybenzenes Benzoyl derivatives Anisoles Alkyl aryl ethers Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: P-methoxybenzoic acid or derivatives - Benzoic acid - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Methoxybenzene - Alkyl aryl ether - Monocarboxylic acid or derivatives - Ether - Carboxylic acid - Carboxylic acid derivative - Organooxygen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.
• External Descriptors: methoxybenzoic acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Alvos associados (humanos)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

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TYR Tclin Tyrosinase (717 Activities)

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CA1 Tclin Carbonic anhydrase I (13240 Activities)

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TPMT Tchem Thiopurine S-methyltransferase (45 Activities)

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Alvos associados (não humanos)

Rattus norvegicus (775804 Activities)

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RAW264.7 (28094 Activities)

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fabI Enoyl-acyl-carrier protein reductase (415 Activities)

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lpxC UDP-3-O-[3-hydroxymyristoyl] N-acetylglucosamine deacetylase (12 Activities)

Discover Target: lpxC

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clpP ATP-dependent Clp protease proteolytic subunit (245 Activities)

Discover Target: clpP

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Heterodera zeae (651 Activities)

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Mecanismos de ação

Propriedades químicas e físicas

• Ponto de inflamação (°C): 185℃
• Ponto de ebulição (°C): 275-280°C
• Ponto de fusão (°C): 184°C
• Peso molecular: 152.150 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 152.047 Da
• Monoisotopic Mass: 152.047 Da
• Topological Polar Surface Area: 46.500 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 136.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1