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142717-57-5

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142717-57-5 Usage

General Description

Dihydrocurcumenone is a natural compound found in the rhizomes of turmeric plants. It belongs to the class of compounds known as sesquiterpenoids, which are organic compounds that contain three isoprene units. Dihydrocurcumenone has been studied for its potential health benefits, including anti-inflammatory, antioxidant, and anticancer properties. Research suggests that this compound has the ability to inhibit the growth of cancer cells and reduce inflammation. Additionally, dihydrocurcumenone has been investigated for its potential use in pharmaceuticals, cosmetics, and food products due to its various biological activities. Overall, dihydrocurcumenone shows promise as a natural compound with potential therapeutic and commercial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 142717-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142717-57:
(8*1)+(7*4)+(6*2)+(5*7)+(4*1)+(3*7)+(2*5)+(1*7)=125
125 % 10 = 5
So 142717-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O2/c1-9(2)11-7-13-12(6-5-10(3)16)15(13,4)8-14(11)17/h10,12-13,16H,5-8H2,1-4H3/t10-,12+,13+,15-/m0/s1

142717-57-5SDS

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 (1R,6S,7R)-7-[(3S)-3-hydroxybutyl]-6-methyl-3-propan-2-ylidenebicyclo[4.1.0]heptan-4-one

1.2 Other means of identification

Product number -
Other names dihydrocurcumenone

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:142717-57-5 SDS

142717-57-5Downstream Products

142717-57-5Relevant articles and documents

BIOTRANSFORMATION OF GERMACRONE BY SUSPENSION CULTURED CELLS

Sakamoto, Shiho,Tsuchiya, Naoko,Kuroyanagi, Masanori,Ueno, Akira

, p. 1215 - 1220 (2007/10/02)

The transformation of germacrone, a 10-membered ring sesquiterpene, by suspension cultured cells of Lonicera japonica, Bupleurum falcatum, Polygonum tinctorium and Solidago altissima, was investigated.Germacrone was converted into several types of sesquiterpenes, such as guaiane, eudesman and seco-guaiane and their structures were determined from spectral and chemical evidence.The configurations of some of the products were determined by CD spectroscopy.The differences of the kinds of products among the four suspension cultured cells is discussed.

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