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30359-01-4

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30359-01-4 Usage

General Description

Centrolobol is a natural compound found in the stem bark of Centrolobium ochroxylum, a plant native to South America. It belongs to the group of compounds known as 3-benzylcoumarins and has been the subject of research for its potential medicinal properties. Studies have shown that centrolobol exhibits anti-inflammatory, anti-tumor, and anti-fungal activities, making it an interesting candidate for the development of new drugs. Its chemical structure and biological effects have sparked interest in the scientific community, and further research is ongoing to explore its potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 30359-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30359-01:
(7*3)+(6*0)+(5*3)+(4*5)+(3*9)+(2*0)+(1*1)=84
84 % 10 = 4
So 30359-01-4 is a valid CAS Registry Number.

30359-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Centrolobol

1.2 Other means of identification

Product number -
Other names -

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:30359-01-4 SDS

30359-01-4Relevant articles and documents

Absolute Configuration of Platyphylloside and (-)-Centrolobol

Ohta, Shinji,Koyama, Mika,Aoki, Tadashi,Suga, Takayuki

, p. 2423 - 2424 (1985)

The ansolute configuration of platyphylloside was established to be S by 13C NMR spectroscopy.On the basis of this establishment, the S-configuration previously assigned to the chirality at C-3 of (-)-centrolobol was revised to the R-configuration.

Identification of centrolobol as the platyphylloside metabolite responsible for the observed effect on in vitro digestibility of hay

Sunnerheim, Kerstin,Bratt, Katharina

, p. 5869 - 5872 (2007/10/03)

Syntheses of the metabolites from platyphylloside, a phenol causing digestibility inhibition in rumen fluid, have been performed to identify the active metabolite. 1,7-Bis(4′-hydroxyphenyl)-3-heptanone (3-platyphyllone), racemic, and the two enantiomers o

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