tert-Butyl 2,4-dibromobutyrate

Name: <I>tert</I>-Butyl 2,4-dibromobutyrate
Brand: ALDRICH

technical, ≥85% (GC)

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About This Item

Empirical Formula (Hill Notation):

C₈H₁₄Br₂O₂

CAS Number:

77629-96-0

Molecular Weight:

302.00

Beilstein/REAXYS Number:

4660530

MDL number:

MFCD00042954

UNSPSC Code:

12352100

PubChem Substance ID:

329754791

NACRES:

NA.22

Key Documents

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grade

technical

assay

≥85% (GC)

form

liquid

density

1.562 g/mL at 20 °C (lit.)

functional group

bromo
ester

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.[1][2][3]

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

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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)

Aspirin inhibits hepatocellular carcinoma cell proliferation in vitro and in vivo via inducing cell cycle arrest and apoptosis.

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

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