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Merck
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文件

447463

Sigma-Aldrich

11-溴十一酸甲酯

95%

别名:

11-Bromoundecanoic acid methyl ester

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About This Item

线性分子式:
Br(CH2)10CO2CH3
CAS号:
6287-90-7
分子量:
279.21
MDL號碼:
MFCD00045047
分類程式碼代碼:
12352100
PubChem物質ID:
24868342
NACRES:
NA.22

化驗

95%

折射率

n20/D 1.465 (lit.)

bp

115 °C/0.04 mmHg (lit.)

密度

1.157 g/mL at 25 °C (lit.)

SMILES 字串

COC(=O)CCCCCCCCCCBr

InChI

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

InChI 密鑰

HFNPVFKUZYCDIB-UHFFFAOYSA-N

相关类别

應用

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.

儲存類別代碼

10 - Combustible liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves

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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
Studies on ω-Oxidation of Fatty Acids in vitro.
KAMEI S, et al.
Journal of Biochemistry, 56(1), 72-76 (1964)
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
Santanu Jana et al.
Organic letters, 20(21), 6938-6942 (2018-10-24)
Fungal glycolipids emmyguyacins A and B inhibit the pH-dependent conformational change of hemaglutinin A during replication of the Influenza virus. Herein, we report the first total synthesis and structure confirmation of emmyguyacins A and B. Our efficient route, which involves
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