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Merck
CN

684511

16-溴十六烷酸甲酯

97%

别名:

16-溴十六烷酸甲基酯

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关于此项目

经验公式(希尔记法):
C17H33BrO2
化学文摘社编号:
分子量:
349.35
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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产品名称

16-溴十六烷酸甲酯, 97%

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

SMILES string

COC(=O)CCCCCCCCCCCCCCCBr

InChI key

ZYTQDEJMRYPSHE-UHFFFAOYSA-N

assay

97%

form

solid

mp

30-34 °C

functional group

bromo
ester

Quality Level

Application

Omega-官能化长链保护的羧酸。用途:用于自组装单层分子的结构单元。

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

存储类别

11 - Combustible Solids

wgk

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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