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22934-74-3

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22934-74-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22934-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22934-74:
(7*2)+(6*2)+(5*9)+(4*3)+(3*4)+(2*7)+(1*4)=113
113 % 10 = 3
So 22934-74-3 is a valid CAS Registry Number.

22934-74-3SDS

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 4,5,7-trimethoxy-6-prop-2-enyl-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names Radiatinin

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:22934-74-3 SDS

22934-74-3Downstream Products

22934-74-3Relevant articles and documents

Antioxidant Activity of Natural Allylpolyalkoxybenzene Plant Essential Oil Constituents

Samet, Alexander V.,Shevchenko, Oksana G.,Rusak, Vyacheslav V.,Chartov, Eduard M.,Myshlyavtsev, Andrey B.,Rusanov, Daniil A.,Semenova, Marina N.,Semenov, Victor V.

, p. 1451 - 1458 (2019/07/05)

Free-radical-scavenging capacity antioxidant and membrane-protective properties of natural and related synthetic allylpolyalkoxybenzenes with different numbers of alkoxy/methoxy groups in the aromatic ring were evaluated using several in vitro models. These included the DPPH assay, inhibition of lipid peroxidation products accumulation, inhibition of H2O2-induced hemolysis, and oxidation of oxyhemoglobin. A synthetic protocol for the synthesis of natural nothoapiol (9) from a parsley seed metabolite, apiol (7), was developed. A structure-activity relationship study revealed that both the methylenedioxy fragment and methoxy groups in the aromatic ring are favorable for antioxidant activity. Hydroxyapiol (14), containing a hydroxy group in the aromatic core, was identified as the most potent compound. The pentaalkoxy-substituted nothoapiol (9) showed antioxidant activity in mouse brain homogenates, whereas in mouse erythrocytes it exhibited a marked pro-oxidant effect. Despite their low free-radical-scavenging capacity, allylpolyalkoxybenzenes can contribute to the total antioxidant potencies of plant essential oils.

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