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684511

Sigma-Aldrich

Methyl 16-bromohexadecanoate

97%

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Synonym(s):
16-bromohexadecanoic acid, methyl ester
Empirical Formula (Hill Notation):
C17H33BrO2
CAS Number:
Molecular Weight:
349.35
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

solid

mp

30-34 °C

SMILES string

COC(=O)CCCCCCCCCCCCCCCBr

InChI

1S/C17H33BrO2/c1-20-17(19)15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18/h2-16H2,1H3

InChI key

ZYTQDEJMRYPSHE-UHFFFAOYSA-N

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Methyl 16-bromohexadecanoate 97%

684511

Methyl 16-bromohexadecanoate

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Methyl tridecanoate

Methyl 4-iodobenzoate 97%

679100

Methyl 4-iodobenzoate

Methyl thiocyanate 97%

722197

Methyl thiocyanate

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

mp

30-34 °C

mp

5.5 °C (lit.)

mp

112-116 °C

mp

-

form

solid

form

liquid

form

solid

form

liquid

Application

Omega-functionalized long chain protected carboxylic acid. Utility: building block for self-assembled monolayer molecules.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

> 110 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Mukesh K Pandey et al.
Nuclear medicine and biology, 80-81, 13-23 (2019-11-24)
The objectives of the present work were to optimize and validate the synthesis and stability of 14(R,S)-[18F]fluoro-6-thia-heptadecanoic acid ([18F]FTHA) and 16-[18F]fluoro-4-thia-palmitic acid ([18F]FTP) under cGMP conditions for clinical applications. Benzyl-14-(R,S)-tosyloxy-6-thiaheptadecanoate and methyl 16-bromo-4-thia-palmitate were used as precursors for the synthesis
Shane Pawsey et al.
Journal of the American Chemical Society, 125(14), 4174-4184 (2003-04-03)
The structures formed by the adsorption of carboxyalkylphosphonic acids on metal oxides were investigated by (1)H fast magic angle spinning (MAS), heteronuclear correlation (HETCOR), and (1)H double-quantum (DQ) MAS solid-state NMR experiments. The diacids HO(2)C(CH(2))(n)PO(3)H(2) (n = 2, 3, 11

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