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245631

Benzyl bromoacetate

96%

Synonym(s):

Bromoacetic acid benzyl ester

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About This Item

Linear Formula:
BrCH2COOCH2C6H5
CAS Number:
5437-45-6
Molecular Weight:
229.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854747
EC Number:
226-611-4
Beilstein/REAXYS Number:
973658
MDL number:
MFCD00000190
Assay:
96%
Form:
liquid
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Quality Level

200

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

SMILES string

BrCC(=O)OCc1ccccc1

InChI

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

InChI key

JHVLLYQQQYIWKX-UHFFFAOYSA-N

Application

Benzyl bromoacetate was used in the alkylation of (-)-2,3-O-isopropylidene-D-threitol that afforded lipopeptide, 2-[(4R,5R)-5-({[(9H-fluoren-9-yl)methoxy]carbonylaminomethyl}-2,2-dimethyl-1,3-dioxolan-4-yl)methoxy]acetic acid.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBT0822
BCCG9896
BCCF8340
BCBR5080V
BCBR3494V

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Articles

gamma Valerolactone Bio Based Dipolar Aprotic Solvent

Explore gamma-valerolactone (GVL) as a greener solvent replacing DMF, NMP, and DMAc in organic synthesis with efficiency and low toxicity.

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

Global Trade Item Number

SKUGTIN
245631-250G04061825772929
245631-50G04061825772936