Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15835-74-2

Post Buying Request

15835-74-2 Suppliers

Recommended suppliersmore

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

15835-74-2 Usage

Description

Acerosin, also known as 5,7,3'-trihydroxyflavone, is a trihydroxyflavone with methoxy substituents at positions 6, 8, and 4' respectively. It is a naturally occurring compound with potential applications in various industries due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
Acerosin is used as a pharmaceutical compound for its potential therapeutic effects. Its trihydroxyflavone structure and methoxy substituents may contribute to its bioactivity, making it a candidate for further research and development in the field of medicine.
Used in Cosmetic Industry:
In the cosmetic industry, Acerosin may be used as an active ingredient in skincare products due to its antioxidant and anti-inflammatory properties. These properties can help protect the skin from environmental stressors and promote a healthy, youthful appearance.
Used in Food and Beverage Industry:
Acerosin's antioxidant properties may also make it a valuable additive in the food and beverage industry. It could be used to extend the shelf life of products by preventing oxidation and rancidity, as well as to enhance the flavor and color of certain foods and beverages.
Used in Agricultural Industry:
The potential antioxidant and anti-inflammatory properties of Acerosin may also find applications in the agricultural industry. It could be used as a natural pesticide or growth promoter to improve crop yield and protect plants from various diseases.
Used in Research and Development:
Acerosin's unique chemical structure makes it an interesting compound for research and development in various scientific fields. It may be used as a starting material for the synthesis of new compounds with potential applications in medicine, agriculture, and other industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15835-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,3 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15835-74:
(7*1)+(6*5)+(5*8)+(4*3)+(3*5)+(2*7)+(1*4)=122
122 % 10 = 2
So 15835-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O8/c1-23-11-5-4-8(6-9(11)19)12-7-10(20)13-14(21)17(24-2)15(22)18(25-3)16(13)26-12/h4-7,19,21-22H,1-3H3

15835-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name acerosin

1.2 Other means of identification

Product number -
Other names 3',5,7-Trihydroxy-4',6,8-trimethoxyflavone

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:15835-74-2 SDS

15835-74-2Downstream Products

15835-74-2Relevant articles and documents

Semisynthesis of polymethoxyflavonoids from naringin and hesperidin

Li, Yue,Cai, Shuanglian,He, Kailin,Wang, Qiuan

, p. 287 - 290 (2014/06/09)

Polymethoxyflavonoids (PMFs) possess important biological activities, notably as anticancer agents. Semisynthesis of a series of PMFs were performed by glycoside hydrolysis, dehydrogenation, bromination, aromatic nucleophilic substitution, O-methylation, dimethyldioxirane oxidation and regioselective demethylation, starting from abundant and inexpensive natural sources naringin and hesperidin. A new synthetic method for selective methylation using CuBr catalysed and microwave-assisted reaction was developed, and the dimethyl dioxirane oxidation of flavones to flavonols was much improved. The new semisynthetic route has the advantages of easy availability of starting materials, simple operation and good yields.

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 15835-74-2