3-Hexylthiophene - ≥98%, used for 3-Hexylthiophene may be used as starting reagent in the synthesis of poly(3-hexylthiophene) (P3HT). various applications , CAS No.1693-86-3

CAS: 1693-86-3 Cat. No.: H110541 Fórmula: C₁₀H₁₆S Peso molecular: 168.3 Beilstein Registry Number: 1617129 Número CE: 629-237-3

GRADE & PURITY ≥98%

Synonyms

3-n-Hexylthiophene | AM84585 | SB66471 | Thiophene, 3-hexyl- | 3-hexylthiophen | EN300-95564 | BBL102713 | H0756 | 3-Hexylthiophene | 3-hexyl-thiophene | MFCD00143181 | AC-4501 | Q-100204 | AS-19031 | FT-0615787 | AKOS005257744 | GEO-01495 | STL556519 | S

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

Normal

Visão geral

3-Hexylthiophene, a sulfur containing heterocyclic building block, is a thiophene derivative. Poly(3-hexylthiophene) (P3HT) nanofibres have been used for the preparation of organic phototransistors (OPTs).

Specifications

Sinónimos

3-n-Hexylthiophene | AM84585 | SB66471 | Thiophene, 3-hexyl- | 3-hexylthiophen | EN300-95564 | BBL102713 | H0756 | 3-Hexylthiophene | 3-hexyl-thiophene | MFCD00143181 | AC-4501 | Q-100204 | AS-19031 | FT-0615787 | AKOS005257744 | GEO-01495 | STL556519 | S

Especificações e pureza

≥98%

Aplicação

3-Hexylthiophene may be used as starting reagent in the synthesis of poly(3-hexylthiophene) (P3HT).

Condições de armazenamento de armazenamento

Protected from light,Room temperature,Argon charged,Desiccated

Enviado em

Normal

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

488190338

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488190338

Sorrisos canónicos

CCCCCCC1=CSC=C1

IUPAC Name

3-hexylthiophene

InChIKey

JEDHEMYZURJGRQ-UHFFFAOYSA-N

INCHI

1S/C10H16S/c1-2-3-4-5-6-10-7-8-11-9-10/h7-9H,2-6H2,1H3

SMILES isoméricas

CCCCCCC1=CSC=C1

WGK Alemanha

3

Número UN

1993

Peso molecular

168.3

Beilstein

1617129

Reaxy-Rn

1617129

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1617129&ln=

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 Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Heteroaromatic compound - Thiophene - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Descrição: 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

Propriedades químicas e físicas

• Sensibilidade: Light sensitive.Air sensitive
• Índice de refração: 1.496
• Ponto de inflamação (°F): 98.6 °F
• Ponto de inflamação (°C): 37 °C
• Ponto de ebulição (°C): 65°C
• Peso molecular: 168.300 g/mol
• XLogP3: 5.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 168.097 Da
• Monoisotopic Mass: 168.097 Da
• Topological Polar Surface Area: 28.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 90.900
• 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