Tetrahydrofurfuryl Bromide - ≥94%(GC) , CAS No.1192-30-9

CAS: 1192-30-9 Cat. No.: T161718 Peso molecular: 165.03 Beilstein Registry Number: 17(5)1,80 Número EC: 214-750-3 PubChem CID: 14501

GRADE & PURITY ≥94%(GC)

Synonyms

InChI=1/C5H9BrO/c6-4-5-2-1-3-7-5/h5H,1-4H2 | Tetrahydrofurfurylbromide | VOHILFSOWRNVJJ-UHFFFAOYSA- | MFCD00016894 | T1808 | alpha-(Bromomethyl)tetrafuran | SB73883 | DTXSID10870857 | 2-(bromomethyl)oxolane | EINECS 214-750-3 | F0001-0315 | TETRAHYDROFRUF

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

InChI=1/C5H9BrO/c6-4-5-2-1-3-7-5/h5H, 1-4H2 | Tetrahydrofurfurylbromide | VOHILFSOWRNVJJ-UHFFFAOYSA- | MFCD00016894 | T1808 | alpha-(Bromomethyl)tetrafuran | SB73883 | DTXSID10870857 | 2-(bromomethyl)oxolane | EINECS 214-750-3 | F0001-0315 | TETRAHYDROFRUF

Especificaciones y pureza

≥94%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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Pureza

≥94%(GC)

Nombres e identificadores

• Pubchem Sid: 504752561
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752561
• Sonrisas canónicas: C1CC(OC1)CBr
• IUPAC Name: 2-(bromomethyl)oxolane
• InChIKey: VOHILFSOWRNVJJ-UHFFFAOYSA-N
• INCHI: 1S/C5H9BrO/c6-4-5-2-1-3-7-5/h5H,1-4H2
• Isómeros SMILES: C1CC(OC1)CBr
• RTECS: LU6000000
• PubChem CID: 14501
• Peso molecular: 165.03
• Beilstein: 17(5)1,80
• Reaxy-Rn: 102717

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Tetrahydrofurans

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Tetrahydrofurans
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Tetrahydrofurans
• Alternative Parents: Oxacyclic compounds Dialkyl ethers Organobromides Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Tetrahydrofuran - Oxacycle - Ether - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.
• 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

Propiedades químicas y físicas

• Sensibilidad: air &heat sensitive
• Índice de refracción: 1.488
• Punto de inflamación (°F): 73°C(lit.)
• Punto de inflamación (°C): 73°C(lit.)
• Punto de ebullición (°C): 70°C/22mmHg(lit.)
• Peso molecular: 165.030 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 163.984 Da
• Monoisotopic Mass: 163.984 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 56.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Shi Zhiheng, Tang Yongchao, Wei Yue, Liu Guigui, Huang Haolong, Qi Jintu, Feng Zhenfeng, Ye Minghui, Zhang Yufei, Wen Zhipeng, Liu Xiaoqing, Yang Qi, Zhi Chunyi, Li Cheng Chao.  (2026)  Carbon-halogen bond substitution enables high-utilization four-electron iodine redox in noncorrosive dilute electrolytes.  Nature Communications,      [PMID:41723120] [10.1038/s41467-026-69743-z]