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20923-20-0

2-Phenylhydrazono-2-cyanoacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 20923-20-0 Structure

  • Basic information

    1. Product Name: 2-Phenylhydrazono-2-cyanoacetamide
    2. Synonyms: 2-Phenylhydrazono-2-cyanoacetamide
    3. CAS NO:20923-20-0
    4. Molecular Formula: C9H8N4O
    5. Molecular Weight: 188.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20923-20-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Phenylhydrazono-2-cyanoacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Phenylhydrazono-2-cyanoacetamide(20923-20-0)
    11. EPA Substance Registry System: 2-Phenylhydrazono-2-cyanoacetamide(20923-20-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 20923-20-0(Hazardous Substances Data)

20923-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20923-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,2 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20923-20:
(7*2)+(6*0)+(5*9)+(4*2)+(3*3)+(2*2)+(1*0)=80
80 % 10 = 0
So 20923-20-0 is a valid CAS Registry Number.

20923-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1Z)-2-amino-N-anilino-2-oxoethanimidoyl cyanide

1.2 Other means of identification

Product number -
Other names 2-cyano-2-phenylhydrazonoglyoxalic acid amide

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:20923-20-0 SDS

20923-20-0Relevant articles and documents

Synthesis, structures and biological activity of some 4-amino-3-cinnolinecarboxylic acid derivatives, part 1

Stanczak,Kwapiszewski,Lewgowd,Ochocki,Szadowska,Pakulska,Glowka

, p. 884 - 889 (2007/10/02)

This work describes the synthesis of 4-amino-3-cinnolinecarboxamides, which were then hydrolyzed to corresponding 4-amino-3-cinnolinecarboxylic acids. Several compounds were tested for their antibacterial and antifungal activity, and for the central nervous system effect.

STUDIES WITH POLYFUNCTIONALLY SUBSTITUTED HETEROAROMATICS: ARYLHYDRAZONONITRILES FOR THE SYNTHESIS OF POLYFUNCTIONALLY SUBSTITUTED AZINES

Elnagdi, Mohamed Hilmy,Elghandour, Ahmed Hafez Hussien,Harb, Abdel Fattah Ali,Hussien, Abdel Haleem Mostafa,Metwally, Saoud Abdel Meniem

, p. 739 - 750 (2007/10/02)

The reaction of arylhydrazononitriles with naphthols, phenols and glycine is reported.

Synthesis of Azoles and Fused Azoles from α-Arylhydrazononitriles

Ibrahim, Mohamed Kamal Ahmed,El-Moghayar, Mohamed Riffat Hamza

, p. 832 - 835 (2007/10/02)

The reaction of α-arylhydrazononitriles (I) with phenylhydrazine, hydrazine hydrate, p-phenylenediamine, mercaptoacetic acid, and phenyl isothiocyanate gives amidrazone (IIa-c, III), pyrazolone (IVa-c), benzimidazole (X), 4-thiazolone (XIe,d) and 1,2,4-tr

STRUCTURE CHARACTERIZATION OF REACTION PRODUCTS FROM PHENYLHYDRAZONOPROPANEDINITRILE AND THIOLS

Sulo, Pavol,Sturdik, Ernest,Liptaj, Tibor,Jakubik, Tibor,Antalik, Marian

, p. 375 - 382 (2007/10/02)

Phenylhydrazonopropanedinitriles react with thiols (benzyl mercaptan, cysteine, 2-mercaptoethanol, mercaptoacetic acid, glutathione, and alcohol dehydrogenase) to give additon products in which thiolate anion is attached to electrophilic carbon atom of cy

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