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Tanacetin, also known as tanacetone or chrysanthenone, is a sesquiterpene lactone found in various plants, particularly in the Asteraceae family. It is a naturally occurring compound with a unique chemical structure, characterized by a tricyclic ring system. Tanacetin has been studied for its potential anti-inflammatory, antioxidant, and antimicrobial properties, which may contribute to its use in traditional medicine and as a starting point for the development of new pharmaceuticals. The compound's biological activities are of interest to researchers, as they may lead to the discovery of new therapeutic applications.

1401-54-3

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1401-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1401-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1401-54:
(6*1)+(5*4)+(4*0)+(3*1)+(2*5)+(1*4)=43
43 % 10 = 3
So 1401-54-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O4/c1-8-4-5-11(16)14(3)7-6-10-9(2)13(17)19-12(10)15(8,14)18/h10-12,16,18H,1-2,4-7H2,3H3/t10-,11+,12-,14-,15-/m0/s1

1401-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3aS,5aS,6R,9aR,9bS)-6,9a-dihydroxy-5a-methyl-3,9-dimethylene-4,5 ,6,7,8,9b-hexahydro-3aH-benzo[g]benzofuran-2-one

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 -
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More Details:1401-54-3 SDS

1401-54-3Downstream Products

1401-54-3Relevant academic research and scientific papers

Biogenetic-type Synthesis of Santonin, Chrysanolide, Dihydrochrysanolide, Tulirinol, Arbusculin-C, Tanacetin, and Artemin

El-Feraly, Farouk S.,Benigni, Daniel A.,McPhail, Andrew T.

, p. 355 - 364 (2007/10/02)

The title compounds were synthsised from their possible biogenetic precursors through hydroperoxide intermediates generated by photo-oxygenation.This route for biological oxygenation may serve as a substitute to epoxidation.The 13C n.m.r. special assignments for all intermediates were made.Single-crystal X-ray analyses unequivocally established the 1S configuration in dihydrochrysanolide (14) and its hydroperoxy-analogue (12).Isomorphous crystals of (12) and (14) belong to the monoclinic system, space group P21, with a = 14.350(6), b = 5.882(3), c = 10.343(3) Angstroem, β = 107.64(2) deg, Z = 2, for (12), and a = 14.461(6), b = 5.887(3), c = 9.698(4) Angstroem, β = 107.44(2) deg, Z = 2, for (14).Least-squares refinement of atomic parameters converged to R 0.040 for (12) and 0.033 for (14) over 1484 and 1300 reflections, respectively, measured by diffractometer.

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