11-Bromo-1-undecene - ≥94%(GC) , CAS No.7766-50-9

CAS: 7766-50-9 Cat. No.: B151980 Molecular Weight: 233.19 EC Number: 622-571-0

GRADE & PURITY ≥94%(GC)

Synonyms

NSC139878 | NSC-139878 | EN300-6767083 | A839156 | 1-bromo-10-undecene | AKOS015836171 | 1-bromoundec-10-ene | SY038269 | FT-0607212 | 11-Bromo-1-undecene, purum, >=95.0% (GC) | 11-Bromo-1-undecene # | undecylenyl bromide | B3576 | SCHEMBL215267 | 11-Brom

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

11-Bromo-1-undecene is a halogenated hydrocarbon. It can be synthesized by employing alkenyl esters or dibromides as starting materials.

Specifications

Synonyms

NSC139878 | NSC-139878 | EN300-6767083 | A839156 | 1-bromo-10-undecene | AKOS015836171 | 1-bromoundec-10-ene | SY038269 | FT-0607212 | 11-Bromo-1-undecene, purum, >=95.0% (GC) | 11-Bromo-1-undecene # | undecylenyl bromide | B3576 | SCHEMBL215267 | 11-Brom

Specifications & Purity

≥94%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥94%(GC)

Names and Identifiers

• Pubchem Sid: 488189258
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189258
• Canonical Smiles: C=CCCCCCCCCCBr
• IUPAC Name: 11-bromoundec-1-ene
• InChIKey: YPLVPFUSXYSHJD-UHFFFAOYSA-N
• INCHI: 1S/C11H21Br/c1-2-3-4-5-6-7-8-9-10-11-12/h2H,1,3-11H2
• Isomeric SMILES: C=CCCCCCCCCCBr
• WGK Germany: 3
• Molecular Weight: 233.19
• Reaxy-Rn: 1753231
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1753231&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organohalogen compounds
    • Class Organobromides

• Kingdom: Organic compounds
• Superclass: Organohalogen compounds
• Class: 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
• Description: 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

Associated Targets(non-human)

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water, 0.2422 mg/L @ 25°C (est).
• Sensitivity: air sensitive
• Refractive Index: 1.468
• Flash Point(°F): 235.4 °F
• Flash Point(°C): 113 °C
• Boil Point(°C): 149-150 °C/35 mmHg
• Molecular Weight: 233.190 g/mol
• XLogP3: 6.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 9
• Exact Mass: 232.083 Da
• Monoisotopic Mass: 232.083 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 89.000
• 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

References

1. Ziyue Ling, Chunji Jiang, Xianda Liu, Yupei Li, Weifeng Zhao, Changsheng Zhao.  (2023)  Histidine-inspired polyacrylonitrile-based adsorbent with excellent hemocompatibility for the simultaneous removal of bacteria and endotoxin in septic blood.  COMPOSITES PART B-ENGINEERING,      [PMID:] [10.1016/j.compositesb.2023.110994]

2. Hong Yang, Ming Xu, Ling-Xiang Guo, Hao-Fan Ji, Jun-Yu Wang, Bao-Ping Lin, Xue-Qin Zhang, Ying Sun.  (2014)  Organocatalysis in polysiloxane gels: a magnetic-stir-bar encapsulated catalyst system prepared by thiol–ene photo-click immobilization.  RSC Advances,  5  (10): (7304-7310).  [PMID:] [10.1039/C4RA16351F]

3. Yu Fang, Qi Shi, Jinping Qu, Xiang Lu.  (2026)  Single molecule coupling of light and thermal for programmable energy storage.  POLYMER,      [PMID:] [10.1016/j.polymer.2026.129684]