1-Tetradecyne - ≥95%(GC) , CAS No.765-10-6

CAS: 765-10-6 Cat. No.: T162707 Fórmula: C₁₄H₂₆ Peso molecular: 194.36 Número CE: 212-139-6 PubChem CID: 69823

GRAU & PUREZA ≥95%(GC)

Synonyms

1-Tetradecyne, >=97.0% | DTXSID4061096 | Tetradecyne | T0761 | (S)-4-N-Boc-piperazine-2-carboxylicacidmethylester | tetradec-1-yne | tetradec-1-yne;DL-Threonine | A839964 | AKOS015836225 | FT-0608313 | 1-C14H26 | EINECS 212-139-6 | D86375 | 1-Tetradecyne

Storage

Room temperature,Argon charged

Shipped In

Normal

Especificações

Sinónimos

1-Tetradecyne, >=97.0% | DTXSID4061096 | Tetradecyne | T0761 | (S)-4-N-Boc-piperazine-2-carboxylicacidmethylester | tetradec-1-yne | tetradec-1-yne;DL-Threonine | A839964 | AKOS015836225 | FT-0608313 | 1-C14H26 | EINECS 212-139-6 | D86375 | 1-Tetradecyne

Especificações e pureza

≥95%(GC)

Condições de armazenamento de armazenamento

Room temperature,Argon charged

Enviado em

Normal

Pureza

≥95%(GC)

Nomes e identificadores

Pubchem Sid

488184409

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488184409

Sorrisos canónicos

CCCCCCCCCCCCC#C

IUPAC Name

tetradec-1-yne

InChIKey

DZEFNRWGWQDGTR-UHFFFAOYSA-N

INCHI

1S/C14H26/c1-3-5-7-9-11-13-14-12-10-8-6-4-2/h1H,4-14H2,2H3

SMILES isoméricas

CCCCCCCCCCCCC#C

WGK Alemanha

3

PubChem CID

69823

Peso molecular

194.36

Reaxy-Rn

1746546

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Acetylides

• Kingdom: Organic compounds
• Superclass: Acetylides
• Classe: Not available
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Acetylides
• Alternative Parents: Terminal alkynes Unsaturated aliphatic hydrocarbons
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetylide - Monosubstituted alkyne - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Alkyne - Acyclic acetylene - Acetylene - Hydrocarbon - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as acetylides. These are compounds arising by replacement of one or both hydrogen atoms of acetylene (ethyne) by a metal or other cationic group. E.g. NaC#CH monosodium acetylide. By extension, analogous compounds derived from terminal acetylenes, RC#CH. The class is limited here to derivatives of acetylene where the hydrogen atom is replaced with an element with similar or lower electronegativity that carbon.
• 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

• Solubilidade: Not miscible with water. soluble in common organic solvents of low polarity
• Sensibilidade: Air sensitive
• Índice de refração: 1.4390 to 1.4410
• Ponto de ebulição (°C): 252°C
• Ponto de fusão (°C): 0 °C
• Peso molecular: 194.360 g/mol
• XLogP3: 6.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 10
• Exact Mass: 194.203 Da
• Monoisotopic Mass: 194.203 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 137.000
• 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