Butyl vinyl ether - analytical standard , CAS No.111-34-2

CAS: 111-34-2 Cat. No.: B123186 Formula: CH₃(CH₂)₃OCH=CH₂ Peso molecolare: 100.16 Beilstein Registry Number: 1560217 Numero EC: 203-860-7

GRADE & PURITY Analytical standard

Synonyms

EINECS 203-860-7 | Shostakovski balsam | UN2352 | A802345 | n-butyl vinylether | n-butylvinylether | BRN 1560217 | Butyl vinyl ether, inhibited [UN2352] [Flammable liquid] | butylvinyl ether | butyl-vinyl ether | Ether butylvinylique | J-002562 | UN 2352

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice,FedEx DG Service

Specifications

Sinonimi

EINECS 203-860-7 | Shostakovski balsam | UN2352 | A802345 | n-butyl vinylether | n-butylvinylether | BRN 1560217 | Butyl vinyl ether, inhibited [UN2352] [Flammable liquid] | butylvinyl ether | butyl-vinyl ether | Ether butylvinylique | J-002562 | UN 2352

Specifiche e purezza

analytical standard

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light,Argon charged

Spedito in

Wet ice,FedEx DG Service

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Standard analitico

Nomi e identificatori

• Pubchem Sid: 528768934
• Sorrisi canonici: CCCCOC=C
• IUPAC Name: 1-ethenoxybutane
• InChIKey: UZKWTJUDCOPSNM-UHFFFAOYSA-N
• INCHI: 1S/C6H12O/c1-3-5-6-7-4-2/h4H,2-3,5-6H2,1H3
• Isomeri SMILES: CCCCOC=C
• WGK Germania: 2
• RTECS: KN5950000
• Numero UN: 2352
• Gruppo di imballaggio: II
• Peso molecolare: 100.16
• Beilstein: 1560217
• Reaxy-Rn: 1560217
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1560217&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organooxygen compounds
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organooxygen compound - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as organooxygen compounds. These are organic compounds containing a bond between a carbon atom and an oxygen 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

Proprietà chimiche e fisiche

• Sensibilità: Heat,Light & Air Sensitive.
• Indice di rifrazione: 1.4
• Punto di infiammabilità (°F): 10.4 °F - closed cup
• Punto di infiammabilità (°C): -12 °C - closed cup
• Punto di ebollizione (°C): 94 °C
• Punto di fusione (°C): -92°C
• Peso molecolare: 100.160 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 100.089 Da
• Monoisotopic Mass: 100.089 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 41.400
• 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

Riferimenti

1. Chen Lv, Lin Du, Shanshan Tang, Narcisse T. Tsona, Shijie Liu, Hailiang Zhao, Wenxing Wang.  (2017)  Matrix isolation study of the early intermediates in the ozonolysis of selected vinyl ethers.  RSC Advances,  7  (31): (19162-19168).  [PMID:] [10.1039/C7RA01011G]