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8-ketoverrucarin A is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74516-63-5

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74516-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74516-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,1 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74516-63:
(7*7)+(6*4)+(5*5)+(4*1)+(3*6)+(2*6)+(1*3)=135
135 % 10 = 5
So 74516-63-5 is a valid CAS Registry Number.

74516-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Verrucarin A mono ketone

1.2 Other means of identification

Product number -
Other names 8-ketoverrucarin A

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:74516-63-5 SDS

74516-63-5Downstream Products

74516-63-5Relevant academic research and scientific papers

Antileukemic Compounds Derived from the Chemical Modification of Macrocyclic Trichothecenes. 1. Derivatives of Verrucarin A

Jarvis, Bruce B.,Stahly, G. Patrick,Pavanasasivam, Gowsala,Mazzola, Eugene P.

, p. 1054 - 1058 (2007/10/02)

Verrucarin A (2) was epoxidized to give the β-9,10-epoxide 7 (major product) and α-9,10-epoxide 9 (minor product).The β-epoxide 7 and its acetate 8 exhibit high in vivo antileukemic activity against P-388 mouse leukemia, whereas 2 and 9 are inactive.Epoxidation of verrucarin B (3) and roridin A (1) to their respective β-9,10-epoxides (11 and 12, respectively) also yields compounds with substantially increased activity.Allylic alcohols derived from 2, α-C8 (20), β-C8 (14), and C16 (15), were synthesized and tested; only 15 exhibited substantial in vivo activity.

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