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2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 300731-04-8 Structure
  • Basic information

    1. Product Name: 2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide)
    2. Synonyms: 2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide)
    3. CAS NO:300731-04-8
    4. Molecular Formula:
    5. Molecular Weight: 278.271
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 300731-04-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide)(300731-04-8)
    11. EPA Substance Registry System: 2,2'-[(2-hydroxy-5-methyl-1,3-phenylene)bis(methanylidene)]bis(hydrazine-1-carboxamide)(300731-04-8)
  • 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: 300731-04-8(Hazardous Substances Data)

300731-04-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 300731-04-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,0,7,3 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 300731-04:
(8*3)+(7*0)+(6*0)+(5*7)+(4*3)+(3*1)+(2*0)+(1*4)=78
78 % 10 = 8
So 300731-04-8 is a valid CAS Registry Number.

300731-04-8Downstream Products

300731-04-8Relevant articles and documents

Dinuclear Nickel(II) and Palladium(II) Complexes in Combination with Different Co-Catalysts as Highly Active Catalysts for the Vinyl/Addition Polymerization of Norbornene

Lozan, Vasile,Lassahn, Paul-Gerhard,Zhang, Cungen,Wu, Biao,Janiak, Christoph,Rheinwald, Gerd,Lang, Heinrich

, p. 1152 - 1164 (2003)

Dinuclear nickel(II) and palladium(II) complexes with Schiff-base ligands (derived form salicylaldehyde condensed with 2-amino-1-alcohols or from 2-hydroxy-5-methylisophthaldialdehyde and pyridine-2-carboxaldehyde condensed with semicarbazide, thiosemicarbazide, carbonodihydrazide, or thiocarbonodihydrazide) can be activated with the co-catalysts methylalumoxane (MAO) or tris(pentafluorophenyl)borane/triethylaluminium, B (C6F 5)3/AlEt3 for the vinyl/addition polymerization of norbornene to reach activities of up to 2.4·107 g polymer/mol(metal)·h (molar ratios metal:AlMAO = 1:100, metal:borane:AlEt3 = 1:9:10). Polymer characterization by GPC gave molar mass distributions of Mw/Mn ≈ 2, thereby indicating a coordination polymerization with a single-site character of the active species.

Tri-color emission and colorimetric recognition of acetate using semicarbazide and thio-semicarbazide derivatives: Experimental and computational studies

Lohar, Sisir,Sinha, Sougata,Ghosh, Subrata,Das, Debasis

, p. 75 - 80 (2016)

Two new fluorescence probes having semicarbazide (DSC) and thio-semicarbazide (DTSC) units have been derived upon reaction with 2-hydroxy-5-methylbenzene-1,3-dialdehyde. Both the probes show excellent selectivity for acetate ion in DMSO medium whereby DTS

Utilization of ultrasonic irradiation as green and effective one-pot protocol to prepare a novel series of bis-2-amino-1, 3, 4-oxa(thia)diazoles and bis-tetrazoles

Arafa, Wael Abdelgayed Ahmed,Abdel-Magied, Ahmed Fawzy

, p. 327 - 340 (2017/12/06)

In an effective and straightforward conversion, bis-semicarbazones and bis-thiosemicarbazones are transformed into a diversity of novel substituted bis-2-amino-1, 3, 4-oxadiazoles and bis-2-amino-1, 3, 4-thiadiazoles, respectively under ultrasonic irradiation. Bis-tetrazoles are obtained from the dialdehydes by sequential reaction with hydroxylamine hydrochloride, phosphorus pentoxide and sodium azide without isolation of the intermediates oximes and nitriles. All the reactions proceed cleanly and smoothly under mild conditions, with short reaction times and broad functional groups possibility. No side reactions were observed.

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