34070
tert-Butyl 2,4-dibromobutyrate
technical, ≥85% (GC)
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C8H14Br2O2
CAS Number:
Molecular Weight:
302.00
Beilstein:
4660530
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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 Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
224.6 °F - closed cup
Flash Point(C)
107 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), 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.
The Journal of Organic Chemistry, 46, 2991-2991 (1981)
H.H. Wassermann et al.
Tetrahedron Letters, 1089-1089 (1979)
The Journal of Organic Chemistry, 46, 2997-2997 (1981)
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