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36705-76-7

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36705-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36705-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36705-76:
(7*3)+(6*6)+(5*7)+(4*0)+(3*5)+(2*7)+(1*6)=127
127 % 10 = 7
So 36705-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N3O/c15-17-14(18)13-9-5-1-3-7-11(9)16-12-8-4-2-6-10(12)13/h1-8H,15H2,(H,17,18)

36705-76-7SDS

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 acridine-9-carbohydrazide

1.2 Other means of identification

Product number -
Other names Acridin-9-carbonsaeure-hydrazid

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:36705-76-7 SDS

36705-76-7Downstream Products

36705-76-7Relevant articles and documents

An acridine hydrazone derivatives and its preparation and use

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Paragraph 0028, (2016/10/10)

The invention provides acridine acylhydrazone derivatives which are characterized in that the structural formula is disclosed in the specification. The invention also provides a preparation method and application of the acridine acylhydrazone derivatives. The preparation method is simple and has high operability. The acridine acylhydrazone derivatives simultaneously contain the two types of active structures acridine and acylhydrazone, and thus, have higher potential bioactivity. The in-vitro antitumor test indicates that the compounds have high inhibiting action on all tested tumor cells and can be further developed as an antineoplastic drug or lead compound.

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