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10180-86-6

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  • Azuleno[6,5-b]furan-2,5-dione,4-(acetyloxy)-3,3a,4,4a,7a,8,9,9a-octahydro-4a,8-dimethyl-3-methylene-,(3aR,4S,4aR,7aR,8R,9aR)-

    Cas No: 10180-86-6

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  • Azuleno[6,5-b]furan-2,5-dione,4-(acetyloxy)-3,3a,4,4a,7a,8,9,9a-octahydro-4a,8-dimethyl-3-methylene-,(3aR,4S,4aR,7aR,8R,9aR)- cas 10180-86-6

    Cas No: 10180-86-6

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10180-86-6 Usage

General Description

The chemical "(3aR,4S,4aR,7aR,8R,9aR)-4a,8-dimethyl-3-methylidene-2,5-dioxo-2,3,3a,4,4a,5,7a,8,9,9a-decahydroazuleno[6,5-b]furan-4-yl acetate" is a complex organic compound with a molecular formula of C17H22O5. It is classified as a diterpene and is commonly found in certain plant species, particularly in the essential oils of several aromatic herbs. This chemical is used in the food and pharmaceutical industries for its various biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties. Additionally, it has been studied for its potential medicinal applications, such as in the treatment of skin disorders, gastrointestinal issues, and respiratory conditions. However, further research is needed to fully understand its mechanisms and potential therapeutic uses.

Check Digit Verification of cas no

The CAS Registry Mumber 10180-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,8 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10180-86:
(7*1)+(6*0)+(5*1)+(4*8)+(3*0)+(2*8)+(1*6)=66
66 % 10 = 6
So 10180-86-6 is a valid CAS Registry Number.

10180-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3aR,5R,5aR,8aR,9S,9aR)-5,8a-dimethyl-1-methylidene-2,8-dioxo-3a,4,5,5a,9,9a-hexahydroazuleno[6,5-b]furan-9-yl] acetate

1.2 Other means of identification

Product number -
Other names 6-O-acetylhelenalin

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:10180-86-6 SDS

10180-86-6Downstream Products

10180-86-6Relevant articles and documents

Herz,Subramanian

, p. 1101,1102 (1972)

Preparation of sesquiterpene lactone derivatives: Cytotoxic activity and selectivity of action

Beer, María F.,Bivona, Augusto E.,Alberti, Andrés Sánchez,Cerny, Natacha,Reta, Guillermo F.,Martín, Víctor S.,Padrón, José M.,Malchiodi, Emilio L.,Sülsen, Valeria P.,Donadel, Osvaldo J.

, (2019)

Cancer is one of the most important causes of death worldwide. Solid tumors represent the great majority of cancers (>90%) and the chemotherapeutic agents used for their treatment are still characterized by variable efficacy and toxicity. Sesquiterpene lactones are a group of naturally occurring compounds that have displayed a diverse range of biological activities including cytotoxic activity. A series of oxygenated and oxy-nitrogenated derivatives (4–15) from the sesquiterpene lactones cumanin (1), helenalin (2), and hymenin (3) were synthesized. The silylated derivatives of helenalin, compounds 13 and 14, were found to be the most active against tumor cell lines, with GI50 values ranging from 0.15 to 0.59 μM. The ditriazolyl cumanin derivative (11) proved to be more active and selective than cumanin in the tested breast, cervix, lung, and colon tumor cell lines. This compound was the least toxic against splenocytes (CC50 = 524.1 μM) and exhibited the greatest selectivity on tumor cell lines. This compound showed a GI50 of 2.3 μM and a SI of 227.9 on WiDr human colon tumor cell lines. Thus, compound 11 can be considered for further studies and is a candidate for the development of new antitumor agents.

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Dominguez,Romo

, p. 1415,1419 (1963)

-

Chemical modification of Britanin and of inuchenolide C

Dzhazin,Adekenov

, p. 698 - 705 (2007/10/03)

Analogs of helenalin possessing a broad spectrum of biological activity have been synthesized from the readily available sesquiterpene lactones britanin and inuchenolide C. Conditions for the hydrolysis, oxidative transformations, and skeletal rearrangements of the pseudoguaianolides that are characteristic for plants of the genus Inula have been studied.

Antineoplastic agents. 34. Helenium autumnale L.

Pettit,Budzinski,Cragg,Brown,Johnston

, p. 1013 - 1016 (2007/10/07)

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