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20566-17-0

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20566-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20566-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,5,6 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20566-17:
(7*2)+(6*0)+(5*5)+(4*6)+(3*6)+(2*1)+(1*7)=90
90 % 10 = 0
So 20566-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H17N3O/c1-9(2)15-12(16)11-6-4-10(5-7-11)8-14-13-3/h4-9,13H,1-3H3,(H,15,16)

20566-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(methylhydrazinylidene)methyl]-N-propan-2-ylbenzamide

1.2 Other means of identification

Product number -
Other names p-formyl-N-isopropylbenzamide methylhydrazone

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:20566-17-0 SDS

20566-17-0Upstream product

20566-17-0Downstream Products

20566-17-0Relevant articles and documents

Indirect oxidation of the antitumor agent procarbazine by tyrosinase-Possible application in designing anti-melanoma prodrugs

Gasowska-Bajger, Beata,Wojtasek, Hubert

, p. 3296 - 3300 (2008)

The interaction of tyrosinase with the anticancer drug procarbazine has been investigated. In the presence of the enzyme alone no oxidation of this dialkylhydrazine above the background level was observed. However, when phenolic substrates (4-tert-butylcatechol or N-acetyl-l-tyrosine) were included in the reaction mixture, procarbazine was rapidly degraded. Oxygen consumption measurements showed that in a mixture both the phenolic substrate and the drug were oxidized. The major product of procarbazine degradation was isolated and identified as azoprocarbazine, the first active metabolite of this drug detected in previous in vivo and in vitro studies. This indirect oxidation of the hydrazine group in this anticancer agent indicates possible application of a hydrazine linker in construction of tyrosinase-activated anti-melanoma prodrugs.

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