Key Documents

View All Documentation

115835

2-Bromoacetophenone

Name: 2-Bromoacetophenone
Brand: ALDRICH

98%

Synonym(s):

ω-Bromoacetophenone, Phenacyl bromide

Select a Size

Change View

About This Item

Linear Formula:

C₆H₅COCH₂Br

CAS Number:

70-11-1

Molecular Weight:

199.04

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24847241

EC Number:

200-724-9

Beilstein/REAXYS Number:

606474

MDL number:

MFCD00000195

Assay:

98%

Form:

solid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

98%

form

solid

bp

135 °C/18 mmHg (lit.)

mp

48-51 °C (lit.)

functional group

bromo, ketone, phenyl

SMILES string

BrCC(=O)c1ccccc1

InChI

1S/C8H7BrO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2

InChI key

LIGACIXOYTUXAW-UHFFFAOYSA-N

Gene Information

human ... PTPN6(5777)

Description

Application

2-Bromoacetophenone has been used in the analysis of organic acids involving the formation of phenacyl derivatives.

Still not finding the right product?

Explore all of our products under 2-Bromoacetophenone

signalword

Danger

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Regulatory Information

危险化学品

This item has

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Articles

Dihydropinene Pinane Greener Solvent for Organic Synthesis

Effective in key synthesis reactions like Knoevenagel condensation, thalidomide synthesis, and Suzuki coupling for sustainable chemical transformations.

Carbohydrate, organic Acid, and amino Acid composition of bacteroids and cytosol from soybean nodules.

J G Streeter

Plant physiology, 85(3), 768-773 (1987-11-01)

Metabolites in Bradyrhizobium japonicum bacteroids and in Glycine max (L.) Merr. cytosol from root nodules were analyzed using an isolation technique which makes it possible to estimate and correct for changes in concentration which may occur during bacteroid isolation. Bacteroid

Nucleophilic heterocyclic carbene as a novel catalyst for cyclopropanation of cyano acrylates.

Anabha E Raveendran et al.

Organic & biomolecular chemistry, 8(4), 901-905 (2010-02-06)

Nucleophilic heterocyclic carbenes (NHCs) have been used for the first time as catalysts in the cyclopropanation of ethyl cyanocinnamates with phenacyl bromide by Michael-initiated ring-closure (MIRC).

Bromoacetophenone-based photonucleases: photoinduced cleavage of DNA by 4'-bromoacetophenone-pyrrolecarboxamide conjugates.

P A Wender et al.

Organic letters, 1(13), 2117-2120 (2000-06-03)

[formula: see text] 4'-Bromoacetophenone derivatives which upon excitation can generate monophenyl radicals capable of hydrogen atom abstraction were investigated as photoinducible DNA cleaving agents. Pyrrolecarboxamide-conjugated 4'-bromoacetophenones were synthesized, and their DNA cleaving activities and sequence selectivities were determined.

View All Related Papers

Global Trade Item Number

SKU	GTIN
115835-5G	04061838703651
115835-100G	04061838703644
115835-500G	04061832489155