1809337-22-1 Usage
Molecular weight
216.20 g/mol
Structure
A benzene ring with two methyl groups (-CH3) at the 2 and 5 positions, two hydroxyl groups (-OH) at the 3 and 4 positions, and a ester group (-COOCH3) at the para position.
Appearance
Pale yellow solid
Solubility
Slightly soluble in water, soluble in organic solvents like ethanol and methanol
Source
Natural product found in various plants and fungi
+ Antioxidant
Yuglanin A has been studied for its ability to neutralize free radicals and prevent oxidative stress.
+ Anti-inflammatory
It has been researched for its potential to reduce inflammation in the body.
+ Photoprotective
It has been investigated for its ability to protect the skin from harmful UV radiation.
+ Anticancer
It has shown potential in inhibiting the growth of certain cancer cells.
+ Pharmaceutical industry
Due to its various health-related properties, yuglanin A could be used in the development of new drugs.
+ Cosmetic industry
Its antioxidant and UV-absorbing properties make it a promising ingredient for personal care and cosmetic products.
+ Further research and development could lead to additional applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1809337-22-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,0,9,3,3 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1809337-22:
(9*1)+(8*8)+(7*0)+(6*9)+(5*3)+(4*3)+(3*7)+(2*2)+(1*2)=181
181 % 10 = 1
So 1809337-22-1 is a valid CAS Registry Number.
1809337-22-1Relevant articles and documents
Synthetic method of high-purity 2,5 - dimethyl -3 and 4 -dihydroxybenzoic acid methyl ester
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Paragraph 0018; 0020; 0021; 0023; 0024; 0025, (2020/06/24)
The present invention discloses a high purity 2,5-dimethyl-3,4-dihydroxy methylbenzoate synthesis method, which comprises: adopting 3,4-dihydroxy-2-methyl methylbenzoate as a raw material, carrying out a Mannich reaction to obtain a first-step product, dissolving the first-step product in an acetic acid solution, adding a catalyst, carrying out morpholine removing at a temperature of 70-150 DEG C under a hydrogen pressure of 20-80 MPa to obtain a crude product, and carrying out recrystallization on the obtained crude product with an acetic acid aqueous solution to obtain the high purity product. According to the present invention, the raw materials are stable and easy to synthesize; the reaction steps are short, the operation is simple, and the requirement on the production equipment is not high; the required production time is short, and the production cost is saved; and the method is suitable for large-scale industrial production and small batch preparation in the laboratory.
