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570-10-5

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570-10-5 Usage

Description

Evernic acid is a naturally occurring organic compound found in various lichens, known for its allergenic properties and potential applications in different industries.

Uses

Used in Pharmaceutical Industry:
Evernic acid is used as a pharmaceutical agent for its potential therapeutic effects. Its presence in lichens has been studied for its potential use in the development of new drugs and treatments.
Used in Cosmetic Industry:
Evernic acid is used as a cosmetic ingredient for its potential skin care benefits. Its presence in lichens has been studied for its potential use in the development of skincare products and formulations.
Used in Allergen Research:
Evernic acid is used as a research tool in allergen studies. Its allergenic properties make it a valuable compound for understanding the mechanisms of allergic reactions and developing treatments for lichen-induced allergies.
Used in Environmental Monitoring:
Evernic acid can be used as a bioindicator in environmental monitoring. Its presence in lichens can provide valuable information about the health of ecosystems and the presence of pollutants or other environmental stressors.

Check Digit Verification of cas no

The CAS Registry Mumber 570-10-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 570-10:
(5*5)+(4*7)+(3*0)+(2*1)+(1*0)=55
55 % 10 = 5
So 570-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O5/c1-13-4-2-5(9)7(8(11)12)6(10)3-4/h2-3,9-10H,1H3,(H,11,12)

570-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-4-methoxy-6-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 2-hydroxy-4-methoxy-6-methyl-

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:570-10-5 SDS

570-10-5Related news

DFT and QTAIM based investigation on the structure and antioxidant behavior of lichen substances Atranorin, EVERNIC ACID (cas 570-10-5) and Diffractaic acid07/12/2019

In this study, the structural and antioxidant behavior of the three lichen-derived natural compounds such as atranorin (AT), evernic acid (EV) and diffractaic acid (DF) has been investigated in the gas and water phase using both B3LYP and M06-2X functional level of density functional theory (DFT...detailed

570-10-5Relevant articles and documents

Photolytic Studies on the Generation and Trapping of 6-Oxomethylidenecyclohexa-2,4-diene-1-one Derivatives with Various Nucleophiles

Mies, Thomas,White, Andrew J. P.,Parsons, Philip J.,Barrett, Anthony G. M.

, (2021/11/17)

α-Oxoketenes and cyclohexadiene α-oxoketenes are reactive intermediates, particularly the latter due to their high re-aromatization potential. In this communication, we report photolytic studies on the generation of such species from 4-OMe and 4-OMOM protected resorcylate dioxinones and their trapping to give resorcylate esters and amides as well as the formation of adducts with enol-ethers as trapping reagents.

Chemical study on Garhwal Himalayan Lichen: Usnea emidotteries

Rawat,Shukla, Vertika,Negi, Sandeep,Pant

, p. 2566 - 2570 (2007/10/03)

Usnea species are medicinally important, so we take unexplored species, Usnea emidotteris. Seven components 2-hydroxy-3-methoxy-4, 6-dimethyl ethyl benzoate, 2, 4-dihydro-xy-3, 6-dimethyl ethyl benzoate, 2-hydroxy-4-methoxy-3, 6-dimethylbezoic acid, usnic

SELECTIVE INHIBITION OF THE BIOSYNTHESIS OF PENICILLIC ACID

Lari, Jalil,Thomas, Robert

, p. 3305 - 3308 (2007/10/02)

5-Chloroorsellinic acid inhibits the formation of penicillic acid by Penicillium cyclopium at sublethal concentrations.

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