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53101-68-1

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53101-68-1 Usage

Chemical structure

A derivative of chromene with four methyl groups (CH3) attached to the ring and two hydroxyl (OH) groups at positions 2 and 6.

Antioxidant properties

The presence of methyl and hydroxyl groups gives the compound its ability to neutralize free radicals and protect cells from damage.

Potential health benefits

Research suggests that chromene derivatives like 2,5,7,8-tetramethyl-3,4-dihydro-2H-chromene-2,6-diol may have health benefits and could be used in the development of new pharmaceuticals and nutraceuticals.

Appearance

Not specified in the material provided.

Check Digit Verification of cas no

The CAS Registry Mumber 53101-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53101-68:
(7*5)+(6*3)+(5*1)+(4*0)+(3*1)+(2*6)+(1*8)=81
81 % 10 = 1
So 53101-68-1 is a valid CAS Registry Number.

53101-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,7,8-tetramethyl-3,4-dihydrochromene-2,6-diol

1.2 Other means of identification

Product number -
Other names 2,6-dihydroxy-2,5,7,8-tetramethylchroman

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:53101-68-1 SDS

53101-68-1Relevant articles and documents

Antioxidant chroman compounds

-

, (2008/06/13)

The (6-hydroxy-chroman-2-yl) acetic or carboxylic acid derivatives useful as antioxidants and a method for preparing these derivatives from hydroquinones and intermediates in this synthesis as well as the use of these derivatives as intermediates in the preparation of optically active alpha-tocopherol.

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