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Merck
CN

128163

Ethyl 3-bromopropionate

98%

Synonym(s):

β-Bromopropionic acid ethyl ester, 2-Ethoxycarbonylethyl bromide, 3-Bromopropanoic acid ethyl ester, 3-Bromopropionic acid ethyl ester, Ethyl β-bromopropionate, Ethyl 3-bromopropanoate

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About This Item

Linear Formula:
BrCH2CH2COOC2H5
CAS Number:
539-74-2
Molecular Weight:
181.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847832
EC Number:
208-724-0
Beilstein/REAXYS Number:
1700933
MDL number:
MFCD00000251
Assay:
98%

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InChI key

FQTIYMRSUOADDK-UHFFFAOYSA-N

InChI

1S/C5H9BrO2/c1-2-8-5(7)3-4-6/h2-4H2,1H3

SMILES string

CCOC(=O)CCBr

assay

98%

refractive index

n20/D 1.452 (lit.)

bp

135-136 °C/50 mmHg (lit.)

solubility

H2O: soluble, alcohol: soluble, benzene: soluble, chloroform: soluble, diethyl ether: soluble

density

1.412 g/mL at 25 °C (lit.)

functional group

bromo, ester

Quality Level

200

Related Categories

Application

Ethyl 3-bromopropionate was used in the preparation of (3′,4′-dimethoxyphenyl)-5-oxopentanoic 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

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCBB1311
BCBB1311V
1050592
S31689
19616DO

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Novel 2-amino-4-aryl-substituted-and 2-amino-4, 5-disubstituted-thiazoles.
Berlin KD and Herd MD.
Proceedings of the Oklahoma Academy of Science, 71, 29-33 (1991)
Chenxi Li et al.
Molecular pharmaceutics, 16(6), 2648-2660 (2019-05-03)
The complement system plays an important role in host innate immunity, and its activation can be exploited as a potential strategy for vaccine adjuvants. Herein, a pH-responsive micellar vaccine platform (COOH-NPs) was developed using a carboxyl-modified diblock copolymer of poly(2-ethyl-2-oxazoline)-poly(d,l-lactide)

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