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1-Phenyl-N,N-bis(1,3-thiazol-2-yl)methanediamine is a complex organic compound with the molecular formula C13H11N5S2. It is characterized by a phenyl ring attached to a central carbon atom, which is connected to two 1,3-thiazol-2-yl groups and two amine groups. 1-phenyl-N,N-bis(1,3-thiazol-2-yl)methanediamine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The presence of the phenyl group provides a hydrophobic character, while the thiazol-2-yl and amine groups contribute to its chemical reactivity and potential for forming coordination complexes. The compound's properties make it a valuable intermediate in the development of new drugs and other chemical products.

5664-49-3

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5664-49-3 Usage

Chemical Structure

Two thiazole rings and a phenyl group attached to a methanediamine backbone

Primary Use

Corrosion inhibitor for copper

Industrial Applications

Cooling water systems, oilfield operations

Function

Forms a protective film on copper surfaces to prevent corrosion and extend equipment lifespan

Properties

High thermal stability, effective at low concentrations

Check Digit Verification of cas no

The CAS Registry Mumber 5664-49-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5664-49:
(6*5)+(5*6)+(4*6)+(3*4)+(2*4)+(1*9)=113
113 % 10 = 3
So 5664-49-3 is a valid CAS Registry Number.

5664-49-3SDS

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 1-phenyl-N,N'-bis(1,3-thiazol-2-yl)methanediamine

1.2 Other means of identification

Product number -
Other names N,N'-Benzyliden-bis(2-aminothiazol)

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:5664-49-3 SDS

5664-49-3Relevant academic research and scientific papers

NHC-Catalyzed Aza-Benzoin Condensation of N, N′-Dipyridin-2-yl Aminals with Aldehydes

Lamb, Justin S.,Takashima, Ryo,Suzuki, Yumiko

, p. 10224 - 10234 (2021/08/16)

α-Amino ketones are useful compounds because of their synthetic utility and bioactivities. After observing the ability of N,N′-dipyridin-2-yl aminals to form imines in situ, the synthesis of α-amino ketones using N,N′-dipyridin-2-yl aminals was proposed.

Formation of azomethines from 2-aminothiazoles and (heterocyclic) aromatic aldehydes

Hopkinson,Meakins,Purcell

, p. 621 - 624 (2007/10/02)

Reexamination of previous work and new studies show that the reactions of 2-aminothiazoles with (heterocyclic) aromatic aldehydes are not straightforward; there are wide divergencies in behaviour between the various amine-aldehyde pairs. Simple efficient

CONDENSATION REACTIONS BETWEEN AROMATIC ALDEHYDES AND SOME HETEROCYCLIC AROMATIC AMINES

Forlani, Luciano,Sintoni, Marina,Todesco, Paolo E.

, p. 229 - 232 (2007/10/02)

1,1-Diamino derivatives are obtained by means of reactions between 2-aminothiazole and aromatic aldehydes carried out in methanol (and in dimethyl sulphoxide).The reaction of amine with the C=N of imine occurs without catalyst and is an easier process than its addition to C=O.This behaviour is also displayed by a number of aromatic heterocycles and homocyclic amines and may be explained by considering the activating effect of the electron-withdrawing group present in the imine moiety.

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