Methiocarb Solution in Methanol - 1000μg/mL in methanol，uncertain：2% , CAS No.2032-65-7

CAS: 2032-65-7 Cat. No.: BWY359283 Fórmula: C₁₁H₁₅NO₂S Peso molecular: 225.31 Beilstein Registry Number: 1881431 Número EC: 217-991-2

GRADE & PURITY 1000μg/mL in methanol，uncertain：2%

Synonyms

METHIOCARB|Mercaptodimethur|2032-65-7|Mesurol|Metmercapturon|Draza|3,5-Dimethyl-4-(methylthio)phenyl methylcarbamate|Methiocarbe|Mesurol Phenol|3,5-Dimethyl-4-(methylthio)phenol methylcarbamate|Bayer 37344|3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

METHIOCARB | Mercaptodimethur | 2032-65-7 | Mesurol | Metmercapturon | Draza | 3,5-Dimethyl-4-(methylthio)phenyl methylcarbamate | Methiocarbe | Mesurol Phenol | 3,5-Dimethyl-4-(methylthio)phenol methylcarbamate | Bayer 37344 | 3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate

Especificaciones y pureza

1000μg/mL in methanol，uncertain：2%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

• Sonrisas canónicas: CC1=CC(=CC(=C1SC)C)OC(=O)NC
• IUPAC Name: (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
• InChIKey: YFBPRJGDJKVWAH-UHFFFAOYSA-N
• INCHI: 1S/C11H15NO2S/c1-7-5-9(14-11(13)12-3)6-8(2)10(7)15-4/h5-6H,1-4H3,(H,12,13)
• Isómeros SMILES: CC1=CC(=CC(=C1SC)C)OC(=O)NC
• WGK Alemania: 3
• RTECS: FC5775000
• Número ONU: 2757
• Grupo de embalaje: I
• Peso molecular: 225.31
• Beilstein: 1881431
• Reaxy-Rn: 1881431
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1881431&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenoxy compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenoxy compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxy compounds
• Alternative Parents: m-Xylenes Thiophenol ethers Alkylarylthioethers Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Carboximidic acids and derivatives Organopnictogen compounds Organooxygen compounds Imines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Aryl thioether - Thiophenol ether - M-xylene - Xylene - Alkylarylthioether - Carboximidic acid derivative - Thioether - Sulfenyl compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Imine - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group.
• External Descriptors: Carbamate insecticides

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

Objetivos asociados (humanos)

ESR1 Tclin Estrogen receptor alpha (17718 Activities)

Discover Target: ESR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

RXRA Tclin Retinoid X receptor alpha (3637 Activities)

Discover Target: RXRA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Faah Anandamide amidohydrolase (3907 Activities)

Discover Target: Faah

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Brassica napus (1186 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)

Discover Target: Nr1i2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Frankliniella occidentalis (90 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Theba pisana (23 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Peso molecular: 225.310 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 225.082 Da
• Monoisotopic Mass: 225.082 Da
• Topological Polar Surface Area: 63.600 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 211.000
• 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

Referencias

1. Hongying Guo, An Chen, Jinghui Zhou, Yijun Li, Xiwen He, Langxing Chen, Yukui Zhang.  (2022)  Efficient Extraction and Determination of Carbamate Pesticides in Vegetables Based on a Covalent Organic Frameworks with Acylamide Sites.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:35016080] [10.1016/j.chroma.2021.462799]

2. MingYan Wang, JunRao Huang, Meng Wang, DongEn Zhang, Jun Chen.  (2013)  Electrochemical nonenzymatic sensor based on CoO decorated reduced graphene oxide for the simultaneous determination of carbofuran and carbaryl in fruits and vegetables.  FOOD CHEMISTRY,      [PMID:24423520] [10.1016/j.foodchem.2013.11.046]

3. Kai Wu, Yunyou Zhou, Tao Li, Junyong Sun, Xiaoqing Xing, Qian Song.  (2012)  Cadmium Tellurium Quantum Dots in Sol-Gel-Derived Silica Spheres Coated with Calix[6]Arene as an Optical Probe for Dalapon.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2012.703740]

4. Xue-Ping Ding, Dong-Bao Tang, Tao Li, Su-Fan Wang, Yun-You Zhou.  (2011)  A novel spectrofluorometric method for the determination of methiocarb using an amphiphilic p-sulfonatocalix[4]arene.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:21737343] [10.1016/j.saa.2011.05.038]

5. Cong Tian, Ning Zhu, Lu Qiao, Man He, Beibei Chen, Zhekuan Wu, Bin Hu.  (2024)  Magnetic covalent organic framework for magnetic solid-phase extraction of carbamate pesticide residues.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.111065]

6. Xinyue Li, Yue Wang, Cheng Chen, Chao Tian, Xiaoli Yu, Jinglei Liu, Qin Li, Shuling Wang.  (2025)  Sustainable biochar derived from waste lotus seedpod for efficient adsorption of residual carbamate pesticides.  Heliyon,      [PMID:] [10.1016/j.heliyon.2025.e42741]