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2-amino-5-chlorobenzophenoneamidinohydrazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134867-99-5

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134867-99-5 Usage

Chemical Type

Hydrazone derivative

Synthesis Use

Used in organic compound synthesis

Biological Activity

Shows potential antibacterial and antifungal properties

Medicinal Chemistry

Holds promise in medicinal chemistry for developing new pharmaceuticals

Research Status

Further research needed for comprehensive understanding of properties and applications

Check Digit Verification of cas no

The CAS Registry Mumber 134867-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,6 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134867-99:
(8*1)+(7*3)+(6*4)+(5*8)+(4*6)+(3*7)+(2*9)+(1*9)=165
165 % 10 = 5
So 134867-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H14ClN5/c15-10-6-7-12(16)11(8-10)13(19-20-14(17)18)9-4-2-1-3-5-9/h1-8H,16H2,(H4,17,18,20)/b19-13+

134867-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(E)-[(2-amino-5-chlorophenyl)-phenylmethylidene]amino]guanidine

1.2 Other means of identification

Product number -
Other names Acbpa hydrazone

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:134867-99-5 SDS

134867-99-5Relevant academic research and scientific papers

Antiarrhythmic active amidinohydrazones of substituted benzophenones. Part 4: Investigations on photoisomerization of (Z)- and (E)-2-amino-5-chlorobenzophenonamidinohydrazone and the corresponding (E)-N-phenylamidinohydrazone

Richter,Schleuder,Geissler,Tomaschewski,Kasbohm

, p. 916 - 918 (2007/10/02)

The title compounds undergo a photoisomerization by irradiation. If the E-isomers are irradiated by light of a wavelength of an absorption maximum typical for them, they can be converted quantitatively to the corresponding Z-isomers. In case that the synt

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