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51864-08-5

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51864-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51864-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,6 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51864-08:
(7*5)+(6*1)+(5*8)+(4*6)+(3*4)+(2*0)+(1*8)=125
125 % 10 = 5
So 51864-08-5 is a valid CAS Registry Number.

51864-08-5SDS

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 6-[1-(hydroxyamino)ethylidene]-3-methoxycyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Ethanone,1-(2-hydroxy-4-methoxyphenyl)-,oxime

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:51864-08-5 SDS

51864-08-5Downstream Products

51864-08-5Relevant articles and documents

Low-dose paeonol derivatives alleviate lipid accumulation

Pao, Kuan-Chuan,Zhao, Jin-Feng,Lee, Tzong-Shyuan,Huang, Ying-Pei,Han, Chien-Chung,Sherlock Huang, Lin-Chiang,Wu, Kou-Hung,Hsu, Ming-Hua

, p. 5652 - 5656 (2015/03/04)

Here, we present a series of novel paeonol derivatives that prevent lipid accumulation at lower doses and exhibit improved water solubility. According to SAR analysis results, 1-(4-methoxy-2-(2-(piperidin-1-yl)ethoxy)phenyl)ethanone (6a) and 4′-methoxy-2′

Synthesis of 1,2-benzisoxazole 2-oxides

Kociolek, Martin G.,Hoermann, Olivia

body text, p. 2632 - 2638 (2012/08/08)

(Chemical Equation Presented) A series of 2-hydroxyaryl ketoximes were converted to the corresponding 1,2- benzisoxazole 2-oxides by treatment with iodobenzene diacetate (in acetic acid or methanol) or N-chlorosuccinimide in water. Both methods gave moderate to excellent yields for a variety of substituted oximes under mild conditions within short reaction times. The latter method has the advantages of an aqueous solvent and lack of halogenated organic by-products. Copyright Taylor & Francis Group, LLC.

Microwave-assisted efficient one-step synthesis of amides from ketones and benzoxazoles from (2-hydroxyaryl) ketones with acetohydroxamic acid using sulfuric acid as the catalyst

Madabhushi, Sridhar,Chinthala, Narsaiah,Vangipuram, Venkata Sairam,Godala, Kondal Reddy,Jillella, Raveendra,Mallu, Kishore Kumar Reddy,Beeram, China Ramanaiah

experimental part, p. 6103 - 6107 (2011/11/30)

Efficient one-step method for the synthesis of amides directly from ketones and benzoxazoles from (2-hydroxyaryl) ketones by the reaction of acetohydroxamic acid using sulfuric acid as catalyst was described.

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