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N-phenyl-N'-tert-butylformamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16596-07-9 Structure
  • Basic information

    1. Product Name: N-phenyl-N'-tert-butylformamidine
    2. Synonyms: N-phenyl-N'-tert-butylformamidine
    3. CAS NO:16596-07-9
    4. Molecular Formula:
    5. Molecular Weight: 176.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16596-07-9.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: N-phenyl-N'-tert-butylformamidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-phenyl-N'-tert-butylformamidine(16596-07-9)
    11. EPA Substance Registry System: N-phenyl-N'-tert-butylformamidine(16596-07-9)
  • 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: 16596-07-9(Hazardous Substances Data)

16596-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16596-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,9 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16596-07:
(7*1)+(6*6)+(5*5)+(4*9)+(3*6)+(2*0)+(1*7)=129
129 % 10 = 9
So 16596-07-9 is a valid CAS Registry Number.

16596-07-9Downstream Products

16596-07-9Relevant articles and documents

A titanium-catalyzed three-component coupling to generate α,β-unsaturated β-iminoamines

Cao, Changsheng,Shi, Yanhui,Odom, Aaron L.

, p. 2880 - 2881 (2003)

The three-component coupling of an amine, alkyne, and isonitrile is facilitated by a titanium complex bearing the N,N-di(pyrrolyl-α-methyl)-N-methylamine (dpma) ligand. From this methodology, α,β-unsaturated β-iminoamines are generated regioselectively with many substrates and are available on multigram scales. Copyright

Imminoamines and preparation thereof

-

Page 9, (2010/02/07)

A process is described for producing one or more substituted iminoamines, in particular β-unsaturated β-iminoamines, in a single reaction comprising reacting one or more primary amines, alkynes, and isonitriles in the presence of a transition metal cataly

A New, Convenient Synthesis of N2-Aryl-N1-alkylformamidines and N2-Aryl-N1,N1-dialkylformamidines

Cereda, Enzo,Bellora, Elio,Donetti, Arturo

, p. 288 - 291 (2007/10/02)

N2-Aryl-N1-alkylformamidines are conveniently and rapidly prepared by the reaction of an aromatic amine with ethyl N-cyanoformamidate to give the N2-aryl-N1-cyanoformamidine.Addition of this intermediate to an e

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