Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5382-85-4

5382-85-4

Post Buying Request

5382-85-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5382-85-4 Usage

General Description

2-(cinnamylideneamino)guanidine is a chemical compound with the formula C10H12N4. It is a guanidine derivative with a cinnamylidene group attached to the amino group. This chemical is commonly used in organic synthesis and as a reagent in chemical reactions. It has been studied for its potential applications in the pharmaceutical industry, particularly in the development of new drugs with antimicrobial and antifungal properties. Additionally, it has been found to have potential in the treatment of certain neurological disorders due to its ability to interact with specific receptor sites in the brain. Overall, 2-(cinnamylideneamino)guanidine has shown promise in various fields of research and is a valuable compound in chemical and pharmaceutical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5382-85-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5382-85:
(6*5)+(5*3)+(4*8)+(3*2)+(2*8)+(1*5)=104
104 % 10 = 4
So 5382-85-4 is a valid CAS Registry Number.

5382-85-4SDS

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)-[(E)-3-phenylprop-2-enylidene]amino]guanidine

1.2 Other means of identification

Product number -
Other names HMS1667O12

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:5382-85-4 SDS

5382-85-4Downstream Products

5382-85-4Relevant 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

Synthesis of aryl-hydrazones via ultrasound irradiation in aqueous medium

Leite, Ana Cristina Lima,Moreira, Diogo Rodrigo de M.,Coelho, Lucas Cunha Duarte,de Menezes, Frederico Duarte,Brondani, Dalci José

, p. 1538 - 1541 (2008/09/19)

The synthesis of aryl-hydrazones from aromatic aldehydes/ketones and hydrazides (semicarbazide, thiosemicarbazide and aminoguanidine) is described using aqueous medium (acid conditions) under ultrasound irradiation with short reaction times (20-30 min), t

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 5382-85-4