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Anilino-guanidine hydrochloride, also known as AGH, is a chemical compound with the molecular formula C7H10ClN5. It is a derivative of guanidine, an organic compound with the formula NH(NH2)2, and aniline, an aromatic amine with the formula C6H5NH2. Anilino-guanidine hydrochloride is a white crystalline solid that is soluble in water and has a melting point of approximately 200°C. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The compound is also known for its potential therapeutic applications, such as its use as an antihypertensive agent and a vasodilator. Due to its reactivity and potential health risks, it is important to handle anilino-guanidine hydrochloride with care and in accordance with proper safety protocols.

4254-63-1

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4254-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4254-63-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4254-63:
(6*4)+(5*2)+(4*5)+(3*4)+(2*6)+(1*3)=81
81 % 10 = 1
So 4254-63-1 is a valid CAS Registry Number.

4254-63-1SDS

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 anilino-guanidine, hydrochloride

1.2 Other means of identification

Product number -
Other names Anilino-guanidin, Hydrochlorid

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:4254-63-1 SDS

4254-63-1Relevant academic research and scientific papers

The reaction studies of α-chloroformylarylhydrazines with thiols, thioureas and α-cyclodiketones

Kuo, Wen-Fa,Wu, Ming-Shyue,Chiu, Chun-Yen,Yeh, Mou-Yung

, p. 215 - 228 (2007/10/03)

The reactions of α-chloroformylarylhydrazines 1 with various types of mercaptan, thiourea and α-cyclodiketone have been studied intensively. 1-Arylhydrazinecarbothioates 2 were obtained via thioesterization when α-chloroformylarylhydrazines reacted with thiols. On the other hand, compounds 3 were obtained when α-chloroformylarylhydrazines reacted with thio-containing heterocyclic compounds, which suggested a totally different mechanism in these types of reactions. Further studies on the reaction of α-chloroformylarylhydrazines 1 with thiourea compounds confirmed a novel cyclization and de-cyclization mechanism, which led to give 2-arylhydrazinecarboximidamides 5 and 1,3,4-thiadiazolin-5-ones 6. In addition, various 1,3,4-oxadiazines 9 were obtained by reacting α-chloroformylarylhydrazines with α-cyclodiketones, showing ring cyclization was involved in this type of reaction.

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