1-Bromodecane - ≥98%(GC) , CAS No.112-29-8

CAS: 112-29-8 Cat. No.: B105788 Molecular Weight: 221.18 Beilstein Registry Number: 1735230 EC Number: 203-955-3

GRADE & PURITY ≥98%(GC)

Synonyms

DTXSID9051581 | Decyl monobromide | FT-0607525 | VS-02933 | SCHEMBL33325 | STL146474 | 1-Bromodecane, 98% | 1-Decyl bromide | Decyl bromide | 1-bromo-n-decane | AKOS005720976 | Q-200114 | Tox21_303974 | CAS-112-29-8 | Y2JDF9ZCB6 | Decylbromide | decylmono

Storage

Protected from light,Room temperature

Shipped In

Normal

Overview

1-Bromodecane participates in alkylation of pentaerythritol and introduces two lipophilic groups in pentaerythritol. It reacts with 1,2-dimethylimidazole to yield 1-decyl-2,3-dimethylimidazolium bromid

Specifications

Synonyms

DTXSID9051581 | Decyl monobromide | FT-0607525 | VS-02933 | SCHEMBL33325 | STL146474 | 1-Bromodecane, 98% | 1-Decyl bromide | Decyl bromide | 1-bromo-n-decane | AKOS005720976 | Q-200114 | Tox21_303974 | CAS-112-29-8 | Y2JDF9ZCB6 | Decylbromide | decylmono

Specifications & Purity

≥98%(GC)

Storage

Protected from light, Room temperature

Shipped In

Normal

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 488180714
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488180714
• Canonical Smiles: CCCCCCCCCCBr
• IUPAC Name: 1-bromodecane
• InChIKey: MYMSJFSOOQERIO-UHFFFAOYSA-N
• INCHI: 1S/C10H21Br/c1-2-3-4-5-6-7-8-9-10-11/h2-10H2,1H3
• Isomeric SMILES: CCCCCCCCCCBr
• WGK Germany: 3
• RTECS: HD6850000
• Molecular Weight: 221.18
• Beilstein: 1735230
• Reaxy-Rn: 1735227
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1735227&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

Chemical and Physical Properties

• Solubility: Miscible with most common organic solvents like ethanol, ethyl ether and chloroform. Not miscible in water.
• Sensitivity: Light sensitive.
• Refractive Index: 1.456
• Flash Point(°F): 201.2 °F
• Flash Point(°C): 94 °C
• Boil Point(°C): 238°C
• Melt Point(°C): -30°C
• Molecular Weight: 221.180 g/mol
• XLogP3: 6.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 8
• Exact Mass: 220.083 Da
• Monoisotopic Mass: 220.083 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 61.900
• 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

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