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113565-15-4

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113565-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113565-15-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,6 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113565-15:
(8*1)+(7*1)+(6*3)+(5*5)+(4*6)+(3*5)+(2*1)+(1*5)=104
104 % 10 = 4
So 113565-15-4 is a valid CAS Registry Number.

113565-15-4SDS

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 Podophyllic Acid

1.2 Other means of identification

Product number -
Other names Epimanool-3,5-dinitro-benzoat

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:113565-15-4 SDS

113565-15-4Related news

Action of Podophyllic Acid (cas 113565-15-4) on malignant tumors—I: Distribution of tritiated Podophyllic Acid (cas 113565-15-4) ethyl hydrazide in subcellular fractions of mouse mammary tumors08/22/2019

The intracellular distribution of radioactivity in mammary tumors has been studied following administration of tritiated podophyllic acid ethyl hydrazide to tumorbearing R III mice. Over 90 per cent of the label is found in the 100,000 g supernatant, two thirds of which is associated with two pr...detailed

Action of Podophyllic Acid (cas 113565-15-4) on malignant tumors—II: Effects of Podophyllic Acid (cas 113565-15-4) ethyl hydrazide on the incorporation of precursors into the nucleic acids of mouse mammary tumors and livers in vivo08/21/2019

Administration of podophyllic acid ethyl hydrazide to mice bearing spontaneous mammary tumors, suppresses the incorporation of radioactive precursors into the nucleic acids of the neoplastic tissue. This suppression was also observed in the case of liver nucleic acids but with exceptions in a nu...detailed

Novel biotransformation process of podophyllotoxin to produce Podophyllic Acid (cas 113565-15-4) and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066, Part II: Process optimization08/20/2019

This work optimized the novel biotransformation process of podophyllotoxin to produce podophyllic acid by Pseudomonas aeruginosa CCTCC AB93066. Firstly, the biotransformation process was significantly affected by medium composition. 5 g/l of yeast extract and 5 g/l of peptone were favorable for ...detailed

113565-15-4Relevant articles and documents

Comprehensive Synthetic Route to Eight Diastereomeric Podophyllum Lignans

Forsey, Steven P.,Rajapaksa, Dayananda,Taylor, Nicholas J.,Rodrigo, Russell

, p. 4280 - 4290 (2007/10/02)

An oxabicyclo compound, 9, prepared in 47percent yield through an isobenzofuran intermediate was converted with excellent regio- and stereocontrol to eight (+/-)-lignan lactones of the podophyllotoxin series.One of the eight, epiisopicropodophyllin, 36, t

TOTAL SYNTHESIS OF (+/-)-PODOPHYLLOTOXIN AND (+/-)-EPIPODOPHYLLOTOXIN.

Eycken, J. Van der,Clercq, P. De,Vandewalle, M.

, p. 3871 - 3874 (2007/10/02)

A novel approach to (+/-)-epipodophyllotoxin (2) and hence also (+/-)-podophyllotoxin (1) is described, involving as a key-step the stereoselective ring closure of the TMS-ester derived from 14a to the tetralin derivative 15 with mesyl chloride.

A stereocontrolled synthesis of antineoplastic podophyllum lignans

Rajapaksa,Rodrigo

, p. 6208 - 6209 (2007/10/02)

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