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32885-81-7

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32885-81-7 Usage

Description

Lasiodiplodin is a natural product derived from the fungus Lasiodiplodia theobromae, known for its potent antifungal and anticancer properties. It has been isolated from various plant sources and has been the subject of several studies due to its potential therapeutic applications.
Used in Pharmaceutical Industry:
Lasiodiplodin is used as an antifungal agent for its strong inhibitory effects against a wide range of fungi, making it a promising candidate for the development of new antifungal medications.
Used in Oncology:
Lasiodiplodin is used as an anticancer agent for its ability to induce apoptosis and inhibit the growth of cancer cells, showing promising anticancer activity.

Check Digit Verification of cas no

The CAS Registry Mumber 32885-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,8 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32885-81:
(7*3)+(6*2)+(5*8)+(4*8)+(3*5)+(2*8)+(1*1)=137
137 % 10 = 7
So 32885-81-7 is a valid CAS Registry Number.

32885-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Lasiodiplodin

1.2 Other means of identification

Product number -
Other names -

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:32885-81-7 SDS

32885-81-7Downstream Products

32885-81-7Relevant articles and documents

Enantiodivergent synthesis of both enantiomers of the macrocyclic lactone lasiodiplodin

Bracher, Franz,Schulte, Brigitte

, p. 2619 - 2622 (1996)

A straightforward approach to both enantiomers of lasiodiplodin 1 is described utilizing (S)-2-(2-hydroxypropyl)-1,3-dithiane 3 as a chiral building block. The key step is a Pd0-catalysed cross coupling of an arene trifluoromethanesulfonate with a 9-alkyl-9-borabicyclo[3.3.1]nonane derivative. The two enantiomers 1 and ent-1 have been obtained in an enantiodivergent manner by macrolactonization of the hydroxy acid 10 with either Gerlach's modification of the Corey lactonization or a Mitsunobu lactonization.

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