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244204-40-8

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244204-40-8 Usage

General Description

Celaphal A is a chemical compound isolated from the natural source of the marine sponge Smenospongia cerebriformis. It belongs to the class of guanidine-containing alkaloids and has been found to exhibit potential cytotoxic and antitumor activities. Celaphal A has been studied for its ability to inhibit the growth of cancer cells by interfering with cell division and inducing apoptosis. Additionally, it has shown promising anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines. These findings suggest that Celaphal A has the potential to be further developed as a therapeutic agent for the treatment of cancer and inflammatory diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 244204-40-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,2,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 244204-40:
(8*2)+(7*4)+(6*4)+(5*2)+(4*0)+(3*4)+(2*4)+(1*0)=98
98 % 10 = 8
So 244204-40-8 is a valid CAS Registry Number.

244204-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,12,13-Trihydroxypodocarpa-5,8,11,13-tetraen-7-one

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:244204-40-8 SDS

244204-40-8Downstream Products

244204-40-8Relevant articles and documents

First total synthesis of (±)-celaphanol A

Bie, Pingyan,Zhang, Chenglu,Li, Anpai,Peng, Xuanjia,Wu, Tongxing,Pan, Xinfu

, p. 581 - 583 (2002)

The first total synthesis of (±)-Celaphanol A was accomplished starting from α-cyclocitral and 3,4-dimethoxy benzyl chloride in six steps. The intramolecular cyclization with BF3·Et2O and enolization in t-BuOK/t-BuOH were the key steps. The process of intramolecular cyclization afforded an all-cis isomer intermediate for synthesis of aromatic tricyclic diterpenes.

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