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3772-56-3

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3772-56-3 Usage

General Description

14-Isopropylpodocarpa-8,11,13-triene-3β,13-diol is a natural compound found in the resin of the New Zealand native tree, Podocarpus totara. It belongs to the class of diterpenoids and has shown various biological activities, including anti-inflammatory, antifungal, and cytotoxic properties. This chemical compound has been studied for its potential pharmaceutical uses and has demonstrated promising results in inhibiting the growth of certain cancer cells. Its unique structure and biological activities make it a valuable compound for further research and potential drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 3772-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3772-56:
(6*3)+(5*7)+(4*7)+(3*2)+(2*5)+(1*6)=103
103 % 10 = 3
So 3772-56-3 is a valid CAS Registry Number.

3772-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3β)-14-Isopropylpodocarpa-8,11,13-triene-3,13-diol

1.2 Other means of identification

Product number -
Other names 19-CARBOXY CHOLESTEROL

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:3772-56-3 SDS

3772-56-3Relevant articles and documents

Synthesis of antimicrobial natural products targeting FtsZ: (+)-totarol and related totarane diterpenes

Kim, Michelle B.,Shaw, Jared T.

supporting information; experimental part, p. 3324 - 3327 (2010/11/02)

(Equation Presented). An efficient, convergent synthesis of totarol by a diastereoselective epoxide/alkene/arene bicyclization is described. The reported synthesis enables the preparation of related diterpenes totaradiol and totarolone as well as previously unavailable derivatives that exhibit comparable inhibition of the bacterial cell division protein FtsZ.

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