Skip to Content
Merck
CN

576743

tert-Butyl 3-bromopropionate

97%

Synonym(s):

2-(tert-Butoxycarbonyl)ethyl bromide, 3-Bromopropionic acid tert-butyl ester

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C7H13BrO2
CAS Number:
Molecular Weight:
209.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

tert-Butyl 3-bromopropionate, 97%

InChI

1S/C7H13BrO2/c1-7(2,3)10-6(9)4-5-8/h4-5H2,1-3H3

SMILES string

CC(C)(C)OC(=O)CCBr

InChI key

RMWVUWLBLWBQDS-UHFFFAOYSA-N

assay

97%

refractive index

n20/D 1.4470 (lit.)

bp

30 °C/0.2 mmHg (lit.)

density

1.253 g/mL at 25 °C (lit.)

functional group

bromo
ester

storage temp.

2-8°C

Application

tert-Butyl 3-bromopropionate may be used to synthesize the following:
  • tert-butyl-12-cholesteryloxi-4,7,10-trioxadodecanoate
  • 2-(tert-butoxycarbonyl)ethyl 2,3,4-tri-O-acetyl-1-thio-α-L-fucopyranoside

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

?Synthesis and characterization of a carboxylic acid derivative for liposomal preparations?
Ionescu C, et al.
Synthesis, 61(04) (2013)
"Synthesis and Biological Evaluation of S-Neofucopeptides as E-and P-Selectin Inhibitors"
Moreno-Vargas.JA, et al.
European Journal of Organic Chemistry, 2008(17), 2973-2982 (2008)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service