All Photos(2)
Synonym(s):
Myristyl bromide, Tetradecyl bromide
Linear Formula:
CH3(CH2)13Br
CAS Number:
Molecular Weight:
277.28
Beilstein:
1742640
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.460 (lit.)
bp
175-178 °C/20 mmHg (lit.)
mp
5-6 °C (lit.)
density
0.932 g/mL at 25 °C (lit.)
SMILES string
CCCCCCCCCCCCCCBr
InChI
1S/C14H29Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15/h2-14H2,1H3
InChI key
KOFZTCSTGIWCQG-UHFFFAOYSA-N
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Related Categories
Application
1-Bromotetradecane was used in the synthesis of:
- tetradecylferrocene
- cationic and zwitterionic gemini surfactants
- metallomesogenic polymers based on bis[η1(N)-3,4-dialkyloxybenzylidene-4′-dodecyloxyaniline]dichloropalladium(II) with octyl, decyl, dodecyl, tetradecyl and hexadecyl alkyl groups
- 9-tetradecylcarbazole
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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R Hernández-Bravo et al.
The journal of physical chemistry. B, 122(15), 4325-4335 (2018-03-29)
A combined study for understanding the molecular interactions of asphaltenes with molecular species such as ionic liquids (ILs) comprised experimental measurements and computational numerical simulation calculations, using density-functional theory (DFT) with dispersion corrections, molecular dynamics (MD) calculations, and experimental rheological
Novel Metallomesogenic Polymers Derived from ? 1-Benzylideneaniline Palladium (II) Complex.
Lee M, et al.
Macromolecules, 32(8), 2777-2782 (1999)
Atakilt Abebe et al.
Bioinorganic chemistry and applications, 2018, 8097483-8097483 (2018-08-18)
New organic salts were synthesized by quaternizing 1,10-phenanthroline using 1-bromotetradecane. The first step yielded an organic salt of formula [C26H37N2]Br. Anion exchange reaction using Li[(CF3SO2)2N] resulted in a more stable salt of formula [C26H37N2][(CF3SO2)2N]. The organic salts were investigated by
Nusrat Jahan et al.
The Journal of organic chemistry, 74(20), 7762-7773 (2009-09-18)
Simple strategies for the synthesis of five series of cationic gemini surfactants and one series of zwitterionic gemini surfactants from pentaerythritol have been developed. Two lipophilic groups were introduced onto pentaerythritol by alkylation of the known compound, O-benzylidenepentaerythritol, with 1-bromooctane
Preparation of a Carbazole-Based Macrocycle Via Precipitation-Driven Alkyne Metathesis.
Zhang W, et al.
Organic Syntheses, 177-191 (2007)
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