Welcome to LookChem.com Sign In|Join Free
  • or
Gaultherin, a natural chemical found in the wintergreen plant (Gaultheria procumbens), is a member of the salicylate class, which shares similarities with aspirin. It is characterized by its minty scent and possesses pain-relieving and anti-inflammatory properties. When metabolized, gaultherin converts into methyl salicylate, which is known for its analgesic and anti-inflammatory effects. Furthermore, gaultherin has been studied for its potential antioxidant and antimicrobial properties.

490-67-5

Post Buying Request

490-67-5 Suppliers

Recommended suppliers

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

490-67-5 Usage

Uses

Used in Pharmaceutical Industry:
Gaultherin is used as a medicinal compound for its pain-relieving and anti-inflammatory properties, similar to aspirin. Its metabolite, methyl salicylate, contributes to its analgesic and anti-inflammatory effects, making it a valuable component in pharmaceutical formulations.
Used in Flavoring Industry:
Gaultherin is used as a flavoring agent for its characteristic minty scent, adding a unique aroma to various food and beverage products.
Used in Antioxidant Applications:
Gaultherin is studied for its potential as an antioxidant, which may help protect cells from damage caused by free radicals and support overall health.
Used in Antimicrobial Applications:
Gaultherin has been investigated for its potential as an antimicrobial agent, which could be utilized in various applications to inhibit the growth of harmful microorganisms.

Check Digit Verification of cas no

The CAS Registry Mumber 490-67-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 490-67:
(5*4)+(4*9)+(3*0)+(2*6)+(1*7)=75
75 % 10 = 5
So 490-67-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O12/c1-27-17(26)8-4-2-3-5-10(8)30-19-16(25)14(23)13(22)11(31-19)7-29-18-15(24)12(21)9(20)6-28-18/h2-5,9,11-16,18-25H,6-7H2,1H3/t9-,11-,12+,13-,14+,15-,16-,18+,19-/m1/s1

490-67-5SDS

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 methyl 2-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxybenzoate

1.2 Other means of identification

Product number -
Other names methyl 2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate

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:490-67-5 SDS

490-67-5Downstream Products

490-67-5Relevant academic research and scientific papers

Synthesis and anti-nociceptive and anti-inflammatory effects of gaultherin and its analogs

Wang, Chao,Zhang, Tian-Tai,Du, Guan-Hua,Zhang, Dong-Ming

, p. 817 - 825 (2011/10/02)

The synthesis of gaultherin (1) and its analogs was carried out to provide 11 glycosides under phase-transfer catalytic conditions. The activities of all synthesized compounds were evaluated by nitric oxide production inhibitory assay in vitro. Methyl 2-O-(4-O-β- d-galactopyranosyl)- β- d-glucopyranosylbenzoate (5f) showed significantly anti-nociceptive and anti-inflammatory effects by the evaluation in vivo. Structure-activity relationships within these compounds were discussed.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 490-67-5