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Merck
CN

447463

11-溴十一酸甲酯

95%

别名:

11-Bromoundecanoic acid methyl ester

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关于此项目

线性分子式:
Br(CH2)10CO2CH3
化学文摘社编号:
分子量:
279.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

11-溴十一酸甲酯, 95%

InChI

1S/C12H23BrO2/c1-15-12(14)10-8-6-4-2-3-5-7-9-11-13/h2-11H2,1H3

SMILES string

COC(=O)CCCCCCCCCCBr

InChI key

HFNPVFKUZYCDIB-UHFFFAOYSA-N

assay

95%

refractive index

n20/D 1.465 (lit.)

bp

115 °C/0.04 mmHg (lit.)

density

1.157 g/mL at 25 °C (lit.)

functional group

bromo
ester

Quality Level

Application

Methyl 11-bromoundecanoate can be used as a reactant to synthesize:
  • Methyl 11-(2,5-dibromophenoxy)undecanoate, which is employed as a precursor to prepare acetylenic cyclophanes.
  • Methyl 11-[(1-phenyl-1H-tetrazol-5-yl)thio]undecanoate, a key intermediate applicable in the synthesis of emmyguyacins side chain.
  • Betain derivatives of 11-bromoundecanoic acid, as potential microbial agents.

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Studies on ω-Oxidation of Fatty Acids in vitro.
KAMEI S, et al.
Journal of Biochemistry, 56(1), 72-76 (1964)
Collins et al.
Organic letters, 2(20), 3189-3192 (2000-09-29)
The synthesis of a series of novel acetylenic cyclophanes is described. X-ray crystallographic analysis of the core structure revealed a twisted conformation with helical chirality. Preliminary results suggest that these cyclophanes, with appropriate functionality, have the potential to act as
A Three Step Synthesis of 11-Cycloheptylundecanoic Acid, a Component of the Thermoacidophile Alicyclobacillus cycloheptanicus.
Hassarajani SA and Mamdapur VR.
Molecules (Basel), 3(2), 41-43 (1998)
Synthesis, characterization, antimicrobial and anti-biofilm activity of a new class of 11-bromoundecanoic acid-based betaines
Yasa SR, et al.
Medicinal Chemistry Research, 26(10), 2592-2601 (2017)
Makoto Hashimoto et al.
Bioorganic & medicinal chemistry letters, 12(1), 89-91 (2001-12-12)
A versatile synthesis of diazirine-based photoreactive fatty acid analogues is reported. The key step is phenoxy alkylation of diazirine with halo alkyl acid esters. The conditions described will be acceptable for the synthesis of various alkyl-length derivatives. The fatty acid

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