882512-68-7 Usage
Description
1-(2,3-Dimethoxy-5-methylphenyl)-2-methylpropan-1-ol, commonly known as Pinoresinol, is a naturally occurring lignan derived from plants such as pine, olive, and sesame. It is recognized for its potential therapeutic properties, which include antioxidant, anti-inflammatory, and anti-cancer effects. Pinoresinol also exhibits anti-bacterial and anti-viral properties, and it is being studied for its possible cardiovascular protective benefits due to its ability to lower blood pressure and reduce cholesterol levels.
Uses
Used in Pharmaceutical Development:
Pinoresinol is used as a potential therapeutic agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It is being investigated for its role in the development of pharmaceuticals targeting various health conditions.
Used in Functional Foods:
Due to its health-promoting properties, Pinoresinol is also being considered for incorporation into functional foods. These foods are designed to provide additional health benefits beyond their basic nutritional value.
Used in Cardiovascular Protection:
Pinoresinol is used as a cardiovascular protective agent because of its ability to lower blood pressure and reduce cholesterol levels, which can help in preventing heart diseases.
Used in Antimicrobial Applications:
Given its anti-bacterial and anti-viral properties, Pinoresinol is also being explored for use in the development of treatments and preventive measures against infectious diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 882512-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,5,1 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 882512-68:
(8*8)+(7*8)+(6*2)+(5*5)+(4*1)+(3*2)+(2*6)+(1*8)=187
187 % 10 = 7
So 882512-68-7 is a valid CAS Registry Number.
882512-68-7Relevant articles and documents
Total synthesis of (±)-herbertenediol
Srikrishna,Satyanarayana
, p. 2892 - 2900 (2007/10/03)
A formal total synthesis of the sesquiterpene (±)-herbertenediol and its dimers mastigophorenes A-D has been accomplished, starting from vanillin via 2,3-dimethoxy-5-methylbenzaldehyde. A combination of Claisen rearrangement and ring-closing metathesis reactions were employed for the generation of the two vicinal quaternary carbons on a cyclopentane ring.
