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5067-26-5

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5067-26-5 Usage

Source

Turmeric plant

Appearance

Vibrant yellow color

Uses

a. Food coloring
b. Flavoring agent

Health Benefits

a. Anti-inflammatory properties
b. Antioxidant properties
c. Anticancer properties

Traditional Medicine

Used for centuries in traditional medicine

Research

Being studied for potential applications in treating various health conditions

Health Conditions

Potentially beneficial for conditions such as arthritis, heart disease, and Alzheimer's disease

Therapeutic Potential

Versatile and valuable chemical compound with promising therapeutic potential

Check Digit Verification of cas no

The CAS Registry Mumber 5067-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5067-26:
(6*5)+(5*0)+(4*6)+(3*7)+(2*2)+(1*6)=85
85 % 10 = 5
So 5067-26-5 is a valid CAS Registry Number.

5067-26-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-hydroxy-3,5-dimethylphenyl)-3-phenylpropane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1-(2-hydroxy-3,5-dimethylphenyl)-3-phenyl-1,3-propanedione

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:5067-26-5 SDS

5067-26-5Relevant articles and documents

PHOTOLYSIS OF CYCLIC ACETALS OF ARYL BENZOYLACETATES AS THE KEY STEP IN A NEW SYNTHESIS OF FLAVONES

Garcia, Hermenegildo,Iborra, Sara,Miranda, Miguel A.,Primo, Jaime

, p. 2511 - 2517 (2007/10/02)

Although the yields found for the photo-Fries rearrangement of the aryl benzoylacetates 1 are poor, blocking of the carbonyl group, as in the related acetal derivatives 3, results in a substantial preparative improvement.Thus, the o-hydroxydibenzoylmethanes 2 are obtained from 1 with an average yield of 18percent, while the corresponding acetals 4 are obtained from 3 with an average yield of 58 percent.Compounds 4 are efficiently converted into flavones 8 by means of wet silica gel, through hydrolysis of the acetal moiety and subsequent cyclization of the resulting o-hydroxydibenzoylmethanes 2.

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