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Merck
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주요 문서

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447463

Sigma-Aldrich

Methyl 11-bromoundecanoate

95%

동의어(들):

11-Bromoundecanoic acid methyl ester

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About This Item

Linear Formula:
Br(CH2)10CO2CH3
CAS Number:
6287-90-7
Molecular Weight:
279.21
MDL number:
MFCD00045047
UNSPSC 코드:
12352100
PubChem Substance ID:
24868342
NACRES:
NA.22

Quality Level

100

분석

95%

refractive index

n20/D 1.465 (lit.)

bp

115 °C/0.04 mmHg (lit.)

density

1.157 g/mL at 25 °C (lit.)

작용기

bromo
ester

SMILES string

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 key

HFNPVFKUZYCDIB-UHFFFAOYSA-N

관련 카테고리

애플리케이션

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.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves

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시험 성적서(COA)

Lot/Batch Number
MKCH3434
SHBK1547
41096DJV
41096DJ
00126ME

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문서 라이브러리 방문

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)
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)
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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