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1,5,11,12-tetrahydroxy-11,20-epoxypicrasa-3,14-diene-2,16-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79752-57-1

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79752-57-1 Usage

Chemical class

Diterpenoids

Source

Natural sources

Biological activities

Diverse, including potential anti-cancer and anti-inflammatory effects

Molecular structure

Unique, characterized by multiple hydroxyl and epoxide groups

Research status

Ongoing, with more research needed to fully understand its bioactivity and potential applications

Mechanism of action

Not fully understood

Therapeutic potential

Promising, but still under investigation

Potential applications

Drug development, based on its medicinal properties

Molecular weight

Approximately 368.43 g/mol

Check Digit Verification of cas no

The CAS Registry Mumber 79752-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,7,5 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79752-57:
(7*7)+(6*9)+(5*7)+(4*5)+(3*2)+(2*5)+(1*7)=181
181 % 10 = 1
So 79752-57-1 is a valid CAS Registry Number.

79752-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name NSC324628

1.2 Other means of identification

Product number -
Other names CHAPARRINONE,5-HYDROXY-14,15-DEHYDRO

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:79752-57-1 SDS

79752-57-1Downstream Products

79752-57-1Relevant academic research and scientific papers

Structural Modifications of Chaparrinone Using Benzeneseleninic Anhydride

Khoi, Nguyen,Polonsky, Judith

, p. 1540 - 1544 (2007/10/02)

Treatment of chaparrinone triacetate with benzeneseleninic anhydride afforded in addition to the Δ14,15-dehydro compound two products arising from angular hydroxylation at C(5).The mechanism of this reaction is discussed.The corresponding deacetylated compounds do not display significant antineoplastic activity.

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