2-Thiophenemethanol - ≥98%(GC) , CAS No.636-72-6

CAS: 636-72-6 Cat. No.: T162809 Formula: C₅H₆OS Peso molecolare: 114.16 Beilstein Registry Number: 383595 Numero EC: 211-264-3 PubChem CID: 69467

GRADE & PURITY ≥98%(GC)

Synonyms

SY036796 | 2-THIENYLCARBINOL | AM804174 | W-104889 | 2-Thienylmethanol | 2-Thiophenemethanol, 98% | EINECS 211-264-3 | Thenyl alcohol | PS-5570 | Thiophene, 2-(hydroxymethyl)- | (thiophen-2-yl)methanol | 2-Hydroxymethylthiophene | 2-hydroxymethyl-thiophen

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinonimi

SY036796 | 2-THIENYLCARBINOL | AM804174 | W-104889 | 2-Thienylmethanol | 2-Thiophenemethanol, 98% | EINECS 211-264-3 | Thenyl alcohol | PS-5570 | Thiophene, 2-(hydroxymethyl)- | (thiophen-2-yl)methanol | 2-Hydroxymethylthiophene | 2-hydroxymethyl-thiophen

Specifiche e purezza

≥98%(GC)

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%(GC)

Nomi e identificatori

• Pubchem Sid: 504754397
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754397
• Sorrisi canonici: C1=CSC(=C1)CO
• IUPAC Name: thiophen-2-ylmethanol
• InChIKey: ZPHGMBGIFODUMF-UHFFFAOYSA-N
• INCHI: 1S/C5H6OS/c6-4-5-2-1-3-7-5/h1-3,6H,4H2
• Isomeri SMILES: C1=CSC(=C1)CO
• WGK Germania: 3
• PubChem CID: 69467
• Peso molecolare: 114.16
• Beilstein: 383595
• Reaxy-Rn: 383596

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Heteroaromatic compounds

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Heteroaromatic compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Heteroaromatic compounds
• Alternative Parents: Thiophenes Primary alcohols Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Heteroaromatic compound - Thiophene - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic heteromonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom.
• External Descriptors: Not available

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

Proprietà chimiche e fisiche

• Sensibilità: air sensitive
• Indice di rifrazione: 1.563
• Punto di infiammabilità (°F): 230°F
• Punto di infiammabilità (°C): >110°C
• Punto di ebollizione (°C): 207°C
• Punto di fusione (°C): 0℃
• Peso molecolare: 114.170 g/mol
• XLogP3: 0.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 114.014 Da
• Monoisotopic Mass: 114.014 Da
• Topological Polar Surface Area: 48.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 56.000
• 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

Riferimenti

1. An Zhidong, Yang Piaoping, Duan Delong, Li Jiang, Wan Tong, Kong Yue, Caratzoulas Stavros, Xiang Shuting, Liu Jiaxing, Huang Lei, Frenkel Anatoly I., Jiang Yuan-Ye, Long Ran, Li Zhenxing, Vlachos Dionisios G..  (2023)  Highly active, ultra-low loading single-atom iron catalysts for catalytic transfer hydrogenation.  Nature Communications,  14  (1): (1-12).  [PMID:37863924] [10.1038/s41467-023-42337-9]

2. Zhang Guofu, Zhang Guihua, Lei Jie, Li Shasha, Xu Shengjun, Ding Chengrong, Shan Shang.  (2016)  Aerobic alcohol ammoxidation catalyzed by copper(I)/amino acid: a scalable protocol to nitriles.  CHEMICAL RESEARCH IN CHINESE UNIVERSITIES,  32  (4): (586-593).  [PMID:] [10.1007/s40242-016-6067-9]

3. Cheng-Long Li, Rui-Ping Zhang, Lu Hou, An-Hui Lu.  (2025)  Pd Supported on Surface Sulfur-Doped Mesoporous Monolithic Carbon to Boost Semihydrogenation of Alkynols.  ChemCatChem,      [PMID:] [10.1002/cctc.202501282]

4. Wenhua Xue, Jian Ye, Zhi Zhu, Reeti Kumar, Jun Zhao.  (2024)  Harnessing trace water for enhanced photocatalytic oxidation of biomass-derived alcohols to aldehydes.  Energy & Environmental Science,      [PMID:] [10.1039/D4EE02301C]

Domande frequenti

What is the purity of this product, and how is it determined?

This product is supplied at ≥98% purity, determined by gas chromatography (GC). Lot-specific values are stated on the Certificate of Analysis.

How should this product be stored?

Store at 2–8 °C under argon. It is supplied under an argon blanket; reseal under inert gas after each use.

How is this product shipped?

This product ships chilled on wet ice. Unpack on arrival and transfer it to the storage condition stated above.

What are the CAS number, molecular formula and molecular weight?

The CAS Number is 636-72-6, the molecular formula is C5H6OS, and the molecular weight is 114.16 g/mol. InChIKey ZPHGMBGIFODUMF-UHFFFAOYSA-N.

What documentation is provided?

Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.