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22107-30-8

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22107-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22107-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22107-30:
(7*2)+(6*2)+(5*1)+(4*0)+(3*7)+(2*3)+(1*0)=58
58 % 10 = 8
So 22107-30-8 is a valid CAS Registry Number.

22107-30-8SDS

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 [1-(6-oxocyclohexa-2,4-dien-1-ylidene)ethylamino]urea

1.2 Other means of identification

Product number -
Other names 2'-hydroxyacetophenone semicarbazone

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:22107-30-8 SDS

22107-30-8Relevant articles and documents

Complexes of 2-hydroxyacetophenone semicarbazones: A novel series of superoxide dismutase mimetics

Safavi, Maliheh,Foroumadi, Alireza,Nakhjiri, Maryam,Abdollahi, Mohammad,Shafiee, Abbas,Ilkhani, Hoda,Ganjali, Mohammad Reza,Hosseinimehr, Seyed Jalal,Emami, Saeed

scheme or table, p. 3070 - 3073 (2010/07/18)

A series of copper(II) and zinc complexes of 2-hydroxyacetophenone semicarbazones have been prepared and evaluated as superoxide dismutase (SOD) mimetics. The SOD-like activity of parent ligands and complexes were determined by the inhibition of nitroblue tetrazolium (NBT) reduction method, using xanthine/xanthine oxidase as the superoxide radical generator. The obtained results indicate that Cu(II) complexes exhibited the most potent SOD-like activities with the IC50 values ranging from ca. 0.2 to 4 μM. Among copper complexes, 2-hydroxy-4-methoxyacetophenone semicarbazone analog was the most active compounds (IC50 ≈0.2 μM).

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