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13308-88-8

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13308-88-8 Usage

Hydrazine derivative

It is a compound derived from hydrazine (N2H4), which is a colorless gas with a characteristic fish-like smell, and is used in various chemical reactions and applications.

Chlorine-substituted phenyl group

The compound contains a phenyl group (a six-membered carbon ring with a hydrogen atom) that has a chlorine atom attached to it. This substitution can affect the compound's chemical reactivity and properties.

Potential mutagen

2-[(E)-(4-Chlorophenyl)methylidene]-1-hydrazinecarboximidamide is known to potentially cause changes in the genetic material (DNA) of organisms, which can lead to mutations.

Research use

The compound is used in scientific research to study its ability to induce genetic mutations, which can help in understanding the mechanisms of mutation and developing methods to prevent or treat mutation-related diseases.

Industrial applications

It is used in the production of pharmaceuticals (medicines) and agrochemicals (chemicals used in agriculture, such as pesticides and fertilizers), due to its diverse range of properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 13308-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13308-88:
(7*1)+(6*3)+(5*3)+(4*0)+(3*8)+(2*8)+(1*8)=88
88 % 10 = 8
So 13308-88-8 is a valid CAS Registry Number.

13308-88-8SDS

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 2-[(E)-(4-chlorophenyl)methylideneamino]guanidine

1.2 Other means of identification

Product number -
Other names N-Amidino-p-chlorbenzaldehydhydrazon

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:13308-88-8 SDS

13308-88-8Relevant articles and documents

Synthesis, Antileishmanial Activity and In Silico Studies of Aminoguanidine Hydrazones (AGH) and Thiosemicarbazones (TSC) Against Leishmania chagasi Amastigotes

Alexandre-Moreira, Magna S.,Aquino, Pedro G. V.,Bourguignon, Jean-Jacques,Bri-Card, Jacques,Freitas, Johnnatan D.,Meneghetti, Mario R.,Nascimento, Igor J. S.,Queiroz, Aline C.,Rodrigues, Klinger A. F.,Rodrigues, Raiza R. L.,Santos, Mariana S.,Schmitt, Martine,de Aquino, Thiago M.,Araújo, Morgana V.,Fran?a, Paulo H. B.,Rodrigues, érica E. E. S.,Santos-Júnior, Paulo F. S.,da Silva-Júnior, Edeildo F.,de Araújo-Júnior, Jo?o X.

, p. 151 - 169 (2022/02/05)

Background: Leishmaniasis is a worldwide health problem, highly endemic in developing countries. Among the four main clinical forms of the disease, visceral leishmaniasis is the most se-vere, fatal in 95% of cases. The undesired side-effects from first-li

Antiviral compounds. IV. Synthesis and anti influenza virus activity of amidinohydrazones

Nishimura,Yamazaki,Toku,Yoshii,Hasegawa

, p. 2444 - 2447 (2007/10/05)

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