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Methanimidamide, N,N-dimethyl-N'-(5-phenyl-1H-pyrazol-3-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222314-84-3

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222314-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222314-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,3,1 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 222314-84:
(8*2)+(7*2)+(6*2)+(5*3)+(4*1)+(3*4)+(2*8)+(1*4)=93
93 % 10 = 3
So 222314-84-3 is a valid CAS Registry Number.

222314-84-3SDS

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 N,N-dimethyl-N'-(5-phenyl-1H-pyrazol-3-yl)methanimidamide

1.2 Other means of identification

Product number -
Other names 5-phenyl-1H-pyrazol-3-yl-dimethylaminoformamidine

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:222314-84-3 SDS

222314-84-3Relevant academic research and scientific papers

A new synthesis of amino substituted azolo[1,3,5]triazines via reaction of N1,N1-dimethyl-N2-azolylformamidines with cyanamide

Kalinin, Dmitrii V.,Kalinina, Svetlana A.,Dolzhenko, Anton V.

, p. 147 - 154 (2013/03/13)

The amino substituted triazine ring was annelated to aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of azolylformamidines in the reaction of aminoazoles with N,N-dimethylformamide dimethyl acetal followed by the triazine ring closure with cyanamide affording therefore fused aminotriazines.

Synthesis and antimicrobial evaluation of novel pyrazolo[1,5-a]pyrimidine, pyrimido[1,2-a]benzimidazole, triazolo[4,3-a]pyrimidine and pyrido[1,2-a]benzimidazole derivatives incorporated phenylsulfonyl moiety

Shaaban, Mohamed R.

scheme or table, p. 3005 - 3014 (2009/05/27)

Phenylsulfonylacetonitrile (1) reacts with dimethylformamide dimethyl acetal (DMF-DMA) to afford 3-(dimethylamino)-2-(phenylsulfonyl)acrylonitrile (2). Enaminonitrile 2 reacts with 5-aminopyrazole derivatives 3a-e, 5-amino-1,2,4-triazole (7) and 2-aminobenzimidazole (11) to afford new pyrazolo[1,5-a]pyrimidine, triazolo[4,3-a]pyrimidine and pyrimido[1,2-a]benzimidazole derivatives 4a-e, 9 and 12, respectively. Also, 3-(dimethylamino)-2-(phenylsulfonyl)acrylonitrile (2) reacts with 2-(1H-benzimidazol-2-yl)acetonitrile (13) to give the corresponding pyrido[l,2-a]benzimidazole derivative 15. Some of the newly synthesized compounds were tested in vitro for their antibacterial and antifungal activities, and showed promising results.

Polyfunctional fused heterocyclic compounds via indene-1,3-diones

Hassaneen, Hamdi M.,Abdallah, Tayseer A.,Abdelhadi, Hyam A.,Hassaneen, Huwaida M.E.,Pagni, Richard M.

, p. 491 - 497 (2007/10/03)

2-Dimethylaminomethylene- and 2-ethoxymethylene-1,3-indendione 1a,b react with 6-amino-2-thioxopyrimidin-4(3H)-one 2 in boiling acetic acid to give 2-thioxo-1,3-dihydroindeno[3,2-d]pyrimidino[4,5-b]pyridine-4,9-dione (4). The latter compound reacts with h

Heterocyclic Synthesis Via Enaminonitriles: One-Pot Synthesis of Some New Pyrazole, Isoxazole, Pyrimidine, Pyrazolo[1.5-a]pyrimidine, Pyrimido[1,2-a]benzimidazole and Pyrido[1,2a]benzimidazole Derivatives

Dawood, Kamal M.,Farag, Ahmad M.,Kandeel, Zaghloul E.

, p. 537 - 547 (2007/10/03)

A convenient synthesis of some new pyrazole, isoxazole, pyrimidine, pyrazolo[1,5-a]pyrimidine, pyrimido[1,2-a]benzimidazole and pyrido[1,2-a]benzimidazole derivatives is reported.

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