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24211-30-1

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24211-30-1 Usage

Uses

(-)-Farrerol possesses anti-bacterial and anti-inflammatory activities.

Check Digit Verification of cas no

The CAS Registry Mumber 24211-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24211-30:
(7*2)+(6*4)+(5*2)+(4*1)+(3*1)+(2*3)+(1*0)=61
61 % 10 = 1
So 24211-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O5/c1-8-15(20)9(2)17-14(16(8)21)12(19)7-13(22-17)10-3-5-11(18)6-4-10/h3-6,13,18,20-21H,7H2,1-2H3/t13-/m0/s1

24211-30-1 Well-known Company Product Price

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  • Sigma

  • (SML1389)  Farrerol  ≥98% (HPLC)

  • 24211-30-1

  • SML1389-5MG

  • 983.97CNY

  • Detail
  • Sigma

  • (SML1389)  Farrerol  ≥98% (HPLC)

  • 24211-30-1

  • SML1389-25MG

  • 3,970.98CNY

  • Detail

24211-30-1SDS

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 5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one

1.2 Other means of identification

Product number -
Other names matteucinol

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:24211-30-1 SDS

24211-30-1Upstream product

24211-30-1Downstream Products

24211-30-1Relevant articles and documents

Phenolic compounds from the aerial parts of Diplomorpha canescens

Devkota, Hari Prasad,Watanabe, Masato,Watanabe, Takashi,Yahara, Shoji

, p. 554 - 556 (2012)

One new C-methyl flavanone glucoside, farrerol 4′-O-β-D- glucopyranoside (1) was isolated from the aerial parts of Diplomorpha canescens (MEISN.) C. A. MEYER. Fourteen known phenolic compounds such as farrerol (2), luteolin 7-methyl ether 5-O-β-D-glucopyranoside (3), (-)-pinoresinol (4), (-)-lariciresinol (5), (-)-dihydrosesamin (6), (±)-dehydrodiconiferyl alcohol (7), rutarensin (8), umbelliferone (9), coniferyl aldehyde (10), sinapyl aldehyde (11), p-coumaric acid methyl ester (12), p-hydroxybenzaldehyde (13), p-hydroxyacetophenone (14) and syringaldehyde (15) were also isolated for the first time from this plant. Structure of 1 was determined on the basis of spectroscopic data including two dimensional (2D)-NMR, circular dichroism (CD) and by the application of Klyne's rule.

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