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Amarolide is a naturally occurring chemical compound found in the plant Amaroucia caerulea, which belongs to the family Amaranthaceae. It is a sesquiterpene lactone, a type of organic compound derived from terpenes, and is known for its potential anti-inflammatory, anti-cancer, and anti-HIV properties. Amarolide has been the subject of scientific research due to its ability to modulate the activity of certain proteins and enzymes, which may contribute to its therapeutic effects. The compound's structure and biological activities make it a promising candidate for further study in the development of new pharmaceuticals.

29913-86-8

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29913-86-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29913-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,1 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29913-86:
(7*2)+(6*9)+(5*9)+(4*1)+(3*3)+(2*8)+(1*6)=148
148 % 10 = 8
So 29913-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O6/c1-8-5-12(21)18(25)20(4)10(8)6-13-19(3)11(7-14(22)26-13)9(2)15(23)16(24)17(19)20/h8-13,16-17,21,24H,5-7H2,1-4H3/t8-,9-,10+,11+,12+,13-,16-,17+,19-,20+/m1/s1

29913-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2alpha,11alpha)-2,11-Dihydroxypicrasane-1,12,16-trione

1.2 Other means of identification

Product number -
Other names Amarolide

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:29913-86-8 SDS

29913-86-8Downstream Products

29913-86-8Relevant academic research and scientific papers

SYNTHETIC STUDIES ON QUASSINOIDS: TOTAL SYNTHESIS OF (+/-)-AMAROLIDE

Hirota, Hiroshi,Yokoyama, Akihisa,Miyaji, Katsuaki,Nakamura, Toshio,Takahashi, Takeyoshi

, p. 435 - 438 (2007/10/02)

The total synthesis of (+/-)-amarolide (1), a quassinoid having 10 chiral centers, was accomplished from the previously reported 12β-hydroxy-picrasan-3-one (4) by 18 step reactions.

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