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142741-24-0

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142741-24-0 Usage

Uses

Conophylline can be used in pharmacological activity and therapeutic use of differentiation of adipose-derived stem cells into functional islet-like cells using conophlline and nicotinamide.

Check Digit Verification of cas no

The CAS Registry Mumber 142741-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,7,4 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 142741-24:
(8*1)+(7*4)+(6*2)+(5*7)+(4*4)+(3*1)+(2*2)+(1*4)=110
110 % 10 = 0
So 142741-24-0 is a valid CAS Registry Number.

142741-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Conophylline

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:142741-24-0 SDS

142741-24-0Upstream product

142741-24-0Downstream Products

142741-24-0Relevant articles and documents

Biologically active indole and bisindole alkaloids from Tabernaemontana divaricata

Kam, Toh-Seok,Pang, Huey-Shen,Lim, Tuck-Meng

, p. 1292 - 1297 (2003)

The ethanol extract of the leaves of Tabernaemontana divaricata (double flower variety) provided a total of 23 alkaloids, including the new aspidosperma alkaloids, taberhanine, voafinine, N-methylvoafinine, voafinidine, voalenine and the new bisindole alkaloid, conophylinine in addition to the previously known, biologically active bisindole, conophylline and its congener, confoline. The structures of the new alkaloids were established by spectroscopic methods. The preparation and characterization of the corresponding quinones of the biologically active bisindoles are also described in relation to a structure-activity study of these compounds with respect to their action in stimulating insulin expression.

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