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66611-51-6

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66611-51-6 Usage

General Description

2-(naphth-1-yl)acetamide oxime is a chemical compound with the formula C12H11NO2. It is a white to off-white powder that is used as a chelating agent in analytical chemistry and as a reagent in organic synthesis. It is also used in the manufacture of pharmaceuticals and is known for its ability to selectively complex with certain metal ions, such as copper and iron. Additionally, 2-(naphth-1-yl)acetamide oxime has been studied for its potential medicinal properties and has shown promise as an anticancer agent through its ability to inhibit the growth of cancer cells.

Check Digit Verification of cas no

The CAS Registry Mumber 66611-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,1 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66611-51:
(7*6)+(6*6)+(5*6)+(4*1)+(3*1)+(2*5)+(1*1)=126
126 % 10 = 6
So 66611-51-6 is a valid CAS Registry Number.

66611-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(NAPHTH-1-YL)ACETAMIDE OXIME

1.2 Other means of identification

Product number -
Other names 1-naphthyl-acetamidoxime

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:66611-51-6 SDS

66611-51-6Upstream product

66611-51-6Downstream Products

66611-51-6Relevant articles and documents

Synthesis of 4,5-dihydro 1,2,4-oxadiazoles from N-unsubstituted amidoximes

Lessel,Herfs

, p. 22 - 26 (2007/10/03)

4,5-Dihydro 1,2,4-oxadiazoles can be synthesized from aromatic and araliphatic amidoximes by cyclocondensation with aldehydes and ketones. Resulting heterocycles differ in substitution at C-3 and C-5 showing the scope of the simple reaction.

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