1-Bromodocosane - ≥95% , CAS No.6938-66-5

CAS: 6938-66-5 Cat. No.: B152631 Peso molecular: 389.51 Número EC: 230-069-4

GRADE & PURITY ≥95%

Synonyms

n-Docosyl bromide | Docosyl bromide | C22H45Br | DTXSID3064510 | EN300-6494012 | EINECS 230-069-4 | 5-(p-nitrophenyl)-2-furaldehyde;5-(P-Nitrophenyl)-2-furancarbaldehyde | NSC53991 | NSC-53991 | NSC 53991 | SY051880 | 1-Bromodocosane | docosylbromide | Be

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

n-Docosyl bromide | Docosyl bromide | C22H45Br | DTXSID3064510 | EN300-6494012 | EINECS 230-069-4 | 5-(p-nitrophenyl)-2-furaldehyde;5-(P-Nitrophenyl)-2-furancarbaldehyde | NSC53991 | NSC-53991 | NSC 53991 | SY051880 | 1-Bromodocosane | docosylbromide | Be

Especificaciones y pureza

≥95%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 488185954
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185954
• Sonrisas canónicas: CCCCCCCCCCCCCCCCCCCCCCBr
• IUPAC Name: 1-bromodocosane
• InChIKey: QYOXLKAKUAASNA-UHFFFAOYSA-N
• INCHI: 1S/C22H45Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h2-22H2,1H3
• Isómeros SMILES: CCCCCCCCCCCCCCCCCCCCCCBr
• Peso molecular: 389.51
• Reaxy-Rn: 1770458
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1770458&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Clase Organobromides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Clase: Organobromides
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organobromides
• Alternative Parents: Hydrocarbon derivatives Alkyl bromides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organobromide - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as organobromides. These are compounds containing a chemical bond between a carbon atom and a bromine 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

Propiedades químicas y físicas

• Solubilidad: Solubility in Toluene almost transparency
• Punto de fusión (°C): 44 °C
• Peso molecular: 389.500 g/mol
• XLogP3: 12.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 20
• Exact Mass: 388.27 Da
• Monoisotopic Mass: 388.27 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 190.000
• 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

Referencias

1. Haoyu Liu, Jingye Ma, Hong Yuan, Xiang Shi.  (2024)  Catalytic cracking of oleic acid to generate aviation kerosene using platinum–modified ZSM–5 nanosheets.  JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY,      [PMID:] [10.1002/jctb.7714]

2. Xin Guo, Zhiyuan Wang, Siqi Jiang, Mengwei Li, Jianing Guo, Yu Cui, Xueyang Wei, Baohui Qi, Qizhong Huang, Yanduo Liu, Hongquan Jiang, Yufeng Hu.  (2024)  Inductive effect in amino functionalized ionic liquids modified TS-1 nanosheets for efficiently sunlight-driven CO2 reduction.  FUEL,      [PMID:] [10.1016/j.fuel.2024.131504]