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167118

Sigma-Aldrich

Ethyl 4-bromobutyrate

95%

Synonym(s):

γ-Bromobutyric acid ethyl ester, 1-Bromo-3-(carboethoxy)propane, 3-(Ethoxycarbonyl)propyl bromide, 4-Bromobutanoic acid ethyl ester, 4-Bromobutyric acid ethyl ester, Ethyl γ-bromobutyrate, Ethyl 4-bromobutanoate

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About This Item

Linear Formula:
Br(CH2)3COOC2H5
CAS Number:
2969-81-5
Molecular Weight:
195.05
Beilstein:
1749700
EC Number:
221-005-6
MDL number:
MFCD00000259
UNSPSC Code:
12352100
PubChem Substance ID:
24850193
NACRES:
NA.22

Quality Level

200

Assay

95%

form

liquid

refractive index

n20/D 1.456 (lit.)

bp

80-82 °C/10 mmHg (lit.)

density

1.363 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)CCCBr

InChI

1S/C6H11BrO2/c1-2-9-6(8)4-3-5-7/h2-5H2,1H3

InChI key

XBPOBCXHALHJFP-UHFFFAOYSA-N

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Application

Ethyl 4-bromobutyrate was used in Enzyme-linked immunosorbent assay for zilpaterol. It was used in the synthesis of isosteric thieno[2,3-b]-azepin-4-ones, having anti-tumor activity. It was also used in the synthesis of poly(2,6-dimethyl-1,4-phenylene oxide).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

195.8 °F - closed cup

Flash Point(C)

91 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBG2831V
STBC7665V
S60786V
STBB4079
S60786

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Weilin L Shelver et al.
Journal of agricultural and food chemistry, 52(8), 2159-2166 (2004-04-15)
Zilpaterol is an beta-adrenergic agonist approved for use in cattle in South Africa and Mexico as a growth promoter. It is not currently approved for use in the EU, USA, or Asia. Here, we report the development of an ELISA
R F Koebel et al.
Journal of medicinal chemistry, 18(2), 192-194 (1975-02-11)
In view of the antitumor activity reported for 7,8-dimethylbenzo[b]azepine-2,5-dione, new isosteric thieno[2,3-b]-azepin-4-ones have been prepared by a Dieckmann ring closure reaction. Substituted 2-amino-3-carbethoxythiophenes were tosylated, or benzoylated, and the corresponding sodium salt was alkylated with ethyl 4-bromobutyrate. The resulting product
Prithidipa Sahoo et al.
Bioorganic chemistry, 71, 315-324 (2017-03-14)
Naphthyridine-based fluorescent probe H1 was synthesized and characterized for the quantification and selective detection of Uric Acid (UA) in live cell. In presence of UA, H1 forms the specific host-guest complex mainly through intermolecular hydrogen bonding and aromatic stacking which
Juan J Parajó et al.
Ecotoxicology and environmental safety, 184, 109580-109580 (2019-09-08)
Ionic Liquids (ILs) are generically regarded as environmentally "harmless" and thus, assumed as "non-toxic". However, due to the endless design possibilities, their ecotoxicological profile is still poorly known. An accurate knowledge on the toxicity of a substance is required, under
Functional polymers and sequential copolymers by phase transfer catalysis.
Pugh C and Percec V.
Polym. Bull., 16(6), 513-520 (1986)
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