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150710-72-8

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150710-72-8 Usage

General Description

Calyxamine B is a natural indole alkaloid isolated from the marine sponge Calyx cf. glomera. It is a complex chemical compound with a unique structure and possesses various biological activities. Studies have shown that calyxamine B has potent anti-inflammatory and antioxidant properties, making it a potential candidate for drug development in the treatment of inflammatory and oxidative stress-related diseases. Additionally, it has been reported to exhibit cytotoxic activity against certain cancer cell lines, indicating its potential as an anticancer agent. Calyxamine B's distinctive chemical structure and promising biological activities make it an interesting compound for further study and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 150710-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,1 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 150710-72:
(8*1)+(7*5)+(6*0)+(5*7)+(4*1)+(3*0)+(2*7)+(1*2)=98
98 % 10 = 8
So 150710-72-8 is a valid CAS Registry Number.

150710-72-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,2,6,6-Tetramethyl-4-piperidinylidene)acetone

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150710-72-8 SDS

150710-72-8Downstream Products

150710-72-8Relevant articles and documents

Two-step synthesis and biological evaluation of calyxamines A and B

Meza-León, Rosa-L.,García, Alvaro Dávila,Sartillo-Piscil, Fernando,Quintero, Leticia,Rivadeneyra, Martha Sosa,Cruz-Gregorio, Silvano

, p. 6852 - 6854 (2013)

A two-step synthesis of naturally occurring alkaloids calyxamines A and B featuring a tandem Mannich–aldol condensation reaction under solvent free conditions, and their inhibitory activity against acetylcholinesterase (AChE) is reported.

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