Skip to Content
MilliporeSigma
All Photos(1)

Documents

34070

Sigma-Aldrich

tert-Butyl 2,4-dibromobutyrate

technical, ≥85% (GC)

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H14Br2O2
CAS Number:
Molecular Weight:
302.00
Beilstein/REAXYS Number:
4660530
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical

assay

≥85% (GC)

form

liquid

density

1.562 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

1S/C8H14Br2O2/c1-8(2,3)12-7(11)6(10)4-5-9/h6H,4-5H2,1-3H3

InChI key

IELBUWARMJVXDU-UHFFFAOYSA-N

Application

tert-Butyl 2,4-dibromobutyrate was employed as building block in reaction with primary amines to yield azetidine-2-carboxylates.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

The Journal of Organic Chemistry, 46, 2997-2997 (1981)
The Journal of Organic Chemistry, 46, 2991-2991 (1981)
H.H. Wassermann et al.
Tetrahedron Letters, 1089-1089 (1979)
Tingting Shi et al.
Oncology reports, 44(2), 457-468 (2020-07-07)
Aspirin, a nonsteroidal anti‑inflammatory drug (NSAID), is known to inhibit cell proliferation in a variety of cancers. However, the underlying mechanism of this inhibition remains unknown. We investigated the effects of aspirin on hepatocellular carcinoma (HCC) cells using in vitro and

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