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Merck
CN

245631

溴乙酸苄酯

96%

别名:

苄基溴乙酸酯

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线性分子式:
BrCH2COOCH2C6H5
化学文摘社编号:
分子量:
229.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-611-4
Beilstein/REAXYS Number:
973658
MDL number:
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产品名称

溴乙酸苄酯, 96%

InChI key

JHVLLYQQQYIWKX-UHFFFAOYSA-N

InChI

1S/C9H9BrO2/c10-6-9(11)12-7-8-4-2-1-3-5-8/h1-5H,6-7H2

SMILES string

BrCC(=O)OCc1ccccc1

assay

96%

form

liquid

refractive index

n20/D 1.544 (lit.)

bp

166-170 °C/22 mmHg (lit.)

density

1.446 g/mL at 25 °C (lit.)

functional group

bromo
ester
phenyl

Quality Level

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Application

将溴乙酸苄酯用于 (-)-2,3- O -异亚丙基-D-苏糖醇的烷基化,得到脂肽 2-[(4 R ,5 R )-5-({ [(9 H -芴-9-基)甲氧基] 羰基氨甲基 }-2,2-二甲基-1,3-二氧杂环戊烷-4-基)甲氧基] 乙酸

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

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Toru Masaka et al.
Chemical & pharmaceutical bulletin, 61(11), 1184-1187 (2013-08-28)
A new component for the solid phase peptide synthesis of lipopeptide, 2-[(4R,5R)-5-({[(9H-fluoren-9-yl)methoxy]carbonylaminomethyl}-2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]acetic acid (2), was designed and synthesized from (-)-2,3-O-isopropylidene-D-threitol (3) in 4 steps. The key step was the selective alkylation of 3 with benzyl bromoacetate in the presence of
Michael Kahnt et al.
Molecules (Basel, Switzerland), 24(12) (2019-06-20)
In this study, we report the synthesis of several amine-spacered conjugates of ursolic acid (UA) and 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). Thus, a total of 11 UA-DOTA conjugates were prepared holding various oligo-methylene diamine spacers as well as different substituents at the

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