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1125-67-3

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1125-67-3 Usage

Chemical structure

A derivative of catechol, a naturally occurring organic compound

Natural occurrence

Found in various plants

Pharmaceutical synthesis

Used in the development of antitumor and antimicrobial drugs

Antioxidant properties

Studied for potential use in skin care products

Safety concerns

Phototoxic effects when exposed to sunlight, requiring cautious handling

Check Digit Verification of cas no

The CAS Registry Mumber 1125-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1125-67:
(6*1)+(5*1)+(4*2)+(3*5)+(2*6)+(1*7)=53
53 % 10 = 3
So 1125-67-3 is a valid CAS Registry Number.

1125-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-5-methylbenzene-1,2-diol

1.2 Other means of identification

Product number -
Other names 3-methoxy-5-methyl-pyrocatechol

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:1125-67-3 SDS

1125-67-3Relevant articles and documents

Layer-by-Layer coated tyrosinase: An efficient and selective synthesis of catechols

Guazzaroni, Melissa,Crestini, Claudia,Saladino, Raffaele

experimental part, p. 157 - 166 (2012/02/13)

Agaricus bisporous tyrosinase was immobilized on commercial available epoxy-resin EupergitC250L and then coated by the Layer-by-Layer method (LbL). The two novel heterogeneous biocatalysts were characterized for their morphology, pH and storage stability, kinetic properties (Km, V max, Vmax/Km) and reusability. These biocatalysts were used for the efficient and selective synthesis of bioactive catechols under mild and environmental friendly experimental conditions. Ascorbic acid was added in the reaction medium to inhibit the formation of ortho-quinones, thus avoiding the known enzyme suicide inactivation process. Catechols were obtained mostly in quantitative yields and conversion of substrate. Tyrosinase immobilized on EupergitC250L and coated by the LbL method showed better catalytic activities, higher pH and storage stability, and reusability with respect to immobilized uncoated tyrosinase. Since chemical procedures to synthesize catechols are often expensive and with high environmental impact, the use of immobilized tyrosinase represents an efficient alternative for the preparation of this family of bioactive compounds.

Reaction of superoxide with phenoxyl-type radicals

d'Alessandro, Nicola,Bianchi, Giorgio,Fang, Xingwang,Jin, Famin,Schuchmann, Heinz-Peter,Von Sonntag, Clemens

, p. 1862 - 1867 (2007/10/03)

Radiolytically generated phenoxyl radicals derived from the structurally similar phenols cresol, tyrosine, tyramine and tyrosol were reacted with O2·- [k = (1-4.5) × 109 dm3 mol-1 s-1 by pu

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