Welcome to LookChem.com Sign In|Join Free

CAS

  • or

20084-99-5

Post Buying Request

20084-99-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

20084-99-5 Usage

Description

Cyperol is a versatile sesquiterpenoid chemical compound that is commonly found in the essential oils of plants such as cyperus and cymbopogon species. It is known for its strong anti-inflammatory and anti-spasmodic properties, making it a popular ingredient in traditional medicine and aromatherapy. Cyperol has also been studied for its potential use in treating various health conditions, such as respiratory disorders and skin diseases. Furthermore, it has been shown to possess antioxidant and antimicrobial activities, which contribute to its potential therapeutic applications.

Uses

Used in Traditional Medicine and Aromatherapy:
Cyperol is used as an active ingredient for its anti-inflammatory and anti-spasmodic properties, helping to alleviate various health conditions and promote overall well-being.
Used in Respiratory Disorders Treatment:
Cyperol is used as a therapeutic agent for respiratory disorders, leveraging its anti-inflammatory properties to improve respiratory function and alleviate symptoms.
Used in Skin Disease Treatment:
Cyperol is used as a treatment for skin diseases, taking advantage of its anti-inflammatory and antimicrobial activities to promote skin health and treat various skin conditions.
Used in Antioxidant Applications:
Cyperol is used as an antioxidant, helping to protect cells from damage caused by free radicals and oxidative stress, thus contributing to overall health and wellness.
Used in Antimicrobial Applications:
Cyperol is used as an antimicrobial agent, utilizing its antimicrobial properties to combat infections and promote a healthy microbial balance.

Check Digit Verification of cas no

The CAS Registry Mumber 20084-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,8 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20084-99:
(7*2)+(6*0)+(5*0)+(4*8)+(3*4)+(2*9)+(1*9)=85
85 % 10 = 5
So 20084-99-5 is a valid CAS Registry Number.

20084-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4aS,7R)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-ol

1.2 Other means of identification

Product number -
Other names Cyperol

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:20084-99-5 SDS

20084-99-5Downstream Products

20084-99-5Relevant articles and documents

Method for preparing alpha-cyperone derivatives

-

Paragraph 0012-0013, (2017/08/27)

The invention discloses a method for preparing alpha-cyperone derivatives. The method comprises the steps: taking alpha-cyperone extracted from a traditional Chinese medicine cyperus rotundus as a raw material, reducing by sodium borohydride to obtain (4aS,7R)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalene-2-alcohol, and carrying out a kinetic resolution reaction catalyzed by enzymes to obtain (2R,4aS,7R)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalene-2-alcohol and (2S,4aS,7R)-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalene-2-alcohol. Prochiral ketone in alpha-cyperone is further basically turned into a chiral center, and resolution is further carried out; the method has the characteristics of simple operation, high product yield, good optical purity and the like.

Enzymic Resolution of (+/-)-Unsaturated Cyclic Terpene Alcohols via Asymmetric Hydrolysis of Corresponding Acetates by Microorganisms

Oritani, Takayuki,Yamashita, Kyohei

, p. 2637 - 2642 (2007/10/02)

Asymmetric hydrolysis of the acetates of (+/-)-cis and trans-carveols by microorganisms or their esterase produced chiral cis and trans-carveols and the acetates of their enantiomers.The enantioselectivity of the microbial hydrolysis and the optical purities of the products varied with the species of microorganisms.This method was also applied in separation of diastereomeric mixtures of (-)-carveols and (-)-7-epi-α-cyperols.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 20084-99-5