1-Nonyne - ≥98% , CAS No.3452-09-3

CAS: 3452-09-3 Cat. No.: N100831 Summenformel: C₉H₁₆ Molekulargewicht: 124.22 Beilstein Registry Number: 1(4)1047 EG-Nummer: 222-375-1

QUALITÄT & REINHEIT ≥98%

Synonyms

J-019633 | 1-NONYNE | Q5410405 | InChI=1/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H | 1-C9H16 | non-1-yne | MFCD00009567 | AKOS015836220 | 760V9GP5A1 | DTXSID4063036 | EINECS 222-375-1 | EN300-344264 | Nonyne | N0301 | UNII-760V9GP5A1 | D91672 | 1-Nonyne, 99%

Storage

Store at 2-8°C

Shipped In

Wet ice

Übersicht

description：

1-Nonyne reacts with thianthrene cation radical tetrafluoroborate to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate.

Spezifikationen

Synonyme

J-019633 | 1-NONYNE | Q5410405 | InChI=1/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H | 1-C9H16 | non-1-yne | MFCD00009567 | AKOS015836220 | 760V9GP5A1 | DTXSID4063036 | EINECS 222-375-1 | EN300-344264 | Nonyne | N0301 | UNII-760V9GP5A1 | D91672 | 1-Nonyne, 99%

Spezifikationen & Reinheit

≥98%

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

508807304

Kanonisches Lächeln

CCCCCCCC#C

IUPAC Name

non-1-yne

InChIKey

OSSQSXOTMIGBCF-UHFFFAOYSA-N

INCHI

1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3

Isomere SMILES

CCCCCCCC#C

WGK Deutschland

3

Molekulargewicht

124.22

Beilstein

1(4)1047

Reaxy-Rn

1736573

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1736573&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Acetylides

• Kingdom: Organic compounds
• Superclass: Acetylides
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Insoluble in water.
• Brechungsindex: 1.422
• Flammpunkt (°F): 91°F
• Flammpunkt (°C): 33 °C
• Siedepunkt (°C): 149-151°C
• Schmelzpunkt (°C): -50°C
• Molekulargewicht: 124.220 g/mol
• XLogP3: 4.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 5
• Exact Mass: 124.125 Da
• Monoisotopic Mass: 124.125 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 83.500
• 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