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Ethanone, 2-hydroxy-1-(3-pyridinyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104501-59-9

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104501-59-9 Usage

Synthesis Reference(s)

Synthesis, p. 943, 1985 DOI: 10.1055/s-1985-31394

Check Digit Verification of cas no

The CAS Registry Mumber 104501-59-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,0 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104501-59:
(8*1)+(7*0)+(6*4)+(5*5)+(4*0)+(3*1)+(2*5)+(1*9)=79
79 % 10 = 9
So 104501-59-9 is a valid CAS Registry Number.

104501-59-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-1-pyridin-3-ylethanone

1.2 Other means of identification

Product number -
Other names Ethanone,2-hydroxy-1-(3-pyridinyl)

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:104501-59-9 SDS

104501-59-9Downstream Products

104501-59-9Relevant academic research and scientific papers

Hypervalent Iodine Oxidation of Enol Silyl Ethers using Boron Trifluoride Etherate. A Direct Route to Aryl Hydroxymethyl Ketones

Moriarty, Robert M.,Prakash, Om,Duncan, Michael P.

, p. 943 - 944 (1985)

Enol silyl ethers of acetophenones and acetylpyridines are oxidized to hydroxymethyl aryl ketones (ω-hydroxyacetophenones) and hydroxyacetylpyridines, respectively, using the system iodosobenzene/boron trifluoride etherate/water.

Hypervalent Iodine Oxidation of Silyl Enol Ethers. A Direct Route to α-Hydroxy Ketones

Moriarty, Robert M.,Duncan, Michael P.,Prakash, Om

, p. 1781 - 1784 (2007/10/02)

Hypervalent iodine oxidation of various silyl enol ethers (aromatic, heteroaromatic, and aliphatic) using iodosobenzene-boron trifluoride diethyl ether-water provides a general and direct route for the α-hydroxylation of ketones.The structures of 2-hydroxy- (8) and 3-hydroxy-acetylpyridine (9) are discussed as well as the scope and mechanism of the reaction.

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