1-Tetradecyne - ≥98% , CAS No.765-10-6

CAS: 765-10-6 Cat. No.: T573192 Formule: C₁₄H₂₆ Poids moléculaire: 194.36 Numéro CE: 212-139-6 PubChem CID: 69823

GRADE & PURITY ≥98%

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

Argon charged,Room temperature

Shipped In

Normal

Specifications

Synonymes

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

Spécifications et pureté

≥98%

Conditions de stockage de stockage

Argon charged,Room temperature

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

Pubchem Sid

504754447

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504754447

Sourires canoniques

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

Isomères SMILES

CCCCCCCCCCCCC#C

WGK Allemagne

3

PubChem CID

69823

Poids moléculaire

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
• Description: 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

Propriétés chimiques et physiques

• Solubilité: Not miscible with water. soluble in common organic solvents of low polarity
• Sensibilité: Sensitive to air
• Indice de réfraction: 1.4390 to 1.4410
• Point d'ébullition (°C): 252°C
• Point de fusion (°C): 0 °C
• Poids moléculaire: 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