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6'-ETHOXY-2'-HYDROXYACETOPHENONE 98 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2750-25-6

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2750-25-6 Usage

Preparation

Preparation by reaction of ethyl iodide on 2,6-dihydroxy acetophenone with potassium carbonate in refluxing acetone (64%).

Check Digit Verification of cas no

The CAS Registry Mumber 2750-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2750-25:
(6*2)+(5*7)+(4*5)+(3*0)+(2*2)+(1*5)=76
76 % 10 = 6
So 2750-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-3-13-9-6-4-5-8(12)10(9)7(2)11/h4-6,12H,3H2,1-2H3

2750-25-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-ethoxy-6-hydroxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-6-ethoxyacetophenon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2750-25-6 SDS

2750-25-6Relevant academic research and scientific papers

Ruthenium-Catalyzed Monoalkenylation of Aromatic Ketones by Cleavage of Carbon-Heteroatom Bonds with Unconventional Chemoselectivity

Kondo, Hikaru,Akiba, Nana,Kochi, Takuya,Kakiuchi, Fumitoshi

supporting information, p. 9293 - 9297 (2015/08/06)

Ruthenium-catalyzed selective monoalkenylation of ortho C-O or C-N bonds of aromatic ketones was achieved. The reaction allowed the direct comparison of the relative reactivities of the cleavage of different carbon-heteroatom bonds, thus suggesting an unc

Synthesis and structure-activity relationships of novel IKK-β inhibitors. Part 3: Orally active anti-inflammatory agents

Murata, Toshiki,Shimada, Mitsuyuki,Sakakibara, Sachiko,Yoshino, Takashi,Masuda, Tsutomu,Shintani, Takuya,Sato, Hiroki,Koriyama, Yuji,Fukushima, Keiko,Nunami, Noriko,Yamauchi, Megumi,Fuchikami, Kinji,Komura, Hiroshi,Watanabe, Akihiko,Ziegelbauer, Karl B.,Bacon, Kevin B.,Lowinger, Timothy B.

, p. 4019 - 4022 (2007/10/03)

A series of 2-amino-3-cyano-4-alkyl-6-(2-hydroxyphenyl)pyridine derivatives was synthesized and evaluated as IκB kinase β (IKK-β) inhibitors. Modification of a novel IKK-β inhibitor 1 (IKK-β IC 50=1500nM, Cell IC50=8000nM) at the 4-p

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