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86044-63-5

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86044-63-5 Usage

Molecular weight

296.33 g/mol

Chemical structure

2-[[E-(3-methoxy-4-oxo-1-cyclohexa-2,5-dienylidene)methyl]amino]guanidine, also known as MOCHDA

Type of compound

Guanidine derivative

Potential applications

Medicine and pharmacology, specifically as an anti-cancer agent, anti-inflammatory, and anti-bacterial agent, as well as in the treatment of neurodegenerative diseases.

Mechanism of action

Not fully understood, but has been studied for its ability to inhibit the growth of cancer cells and its potential anti-inflammatory and anti-bacterial properties.

Additional information

Further research is needed to fully understand the potential uses and mechanisms of action of 2-[[E-(3-methoxy-4-oxo-1-cyclohexa-2,5-dienylidene)methyl]amino]guanidine.

Check Digit Verification of cas no

The CAS Registry Mumber 86044-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,4 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86044-63:
(7*8)+(6*6)+(5*0)+(4*4)+(3*4)+(2*6)+(1*3)=135
135 % 10 = 5
So 86044-63-5 is a valid CAS Registry Number.

86044-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[(E)-(3-methoxy-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]amino]guanidine

1.2 Other means of identification

Product number -
Other names vanillylidenamino-guanidine

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:86044-63-5 SDS

86044-63-5Downstream Products

86044-63-5Relevant 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

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