Skip to Content
Merck
CN
All Photos(1)

Documents

199486

Sigma-Aldrich

2-Bromo-2′,4′-dimethoxyacetophenone

96%

Sign Into View Organizational & Contract Pricing

Linear Formula:
(CH3O)2C6H3COCH2Br
CAS Number:
Molecular Weight:
259.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

form

powder

mp

102-104 °C (lit.)

SMILES string

COc1ccc(C(=O)CBr)c(OC)c1

InChI

1S/C10H11BrO3/c1-13-7-3-4-8(9(12)6-11)10(5-7)14-2/h3-5H,6H2,1-2H3

InChI key

PKVBZABQCCQHLD-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2-Bromo-2′,4′-dimethoxyacetophenone inhibited the activity of papain.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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.

Visit the Document Library

P I Clark et al.
European journal of biochemistry, 84(1), 293-299 (1978-03-01)
Photolysis of papain which had been inhibited with 2-bromo-2',4'-dimethoxyacetophenone regenerated papain, but also formed [deltaSer25]-papain (i.e. papain in which the active-site cysteine residue 25 was replaced by dehydroserine) via the intermediate dehydrocysteine analogue, [deltaCys25]-papain. Reduction with sodium borohydride gave [Ser25]papain.

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