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CAS

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127956-56-3

4,5-dihydro-N,N-dimethyl-2-phenyl-1,3-thiazol-4-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127956-56-3 Structure

  • Basic information

    1. Product Name: 4,5-dihydro-N,N-dimethyl-2-phenyl-1,3-thiazol-4-amine
    2. Synonyms:
    3. CAS NO:127956-56-3
    4. Molecular Formula:
    5. Molecular Weight: 206.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127956-56-3.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: 4,5-dihydro-N,N-dimethyl-2-phenyl-1,3-thiazol-4-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4,5-dihydro-N,N-dimethyl-2-phenyl-1,3-thiazol-4-amine(127956-56-3)
    11. EPA Substance Registry System: 4,5-dihydro-N,N-dimethyl-2-phenyl-1,3-thiazol-4-amine(127956-56-3)

  • 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: 127956-56-3(Hazardous Substances Data)

127956-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127956-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127956-56:
(8*1)+(7*2)+(6*7)+(5*9)+(4*5)+(3*6)+(2*5)+(1*6)=163
163 % 10 = 3
So 127956-56-3 is a valid CAS Registry Number.

127956-56-3Downstream Products

127956-56-3Relevant articles and documents

1,5-Dipolar electrocyclizations of thiocarbonyl ylides bearing C=N groups: Reactions of N-[(dimethylamino)methylene]thiobenzamide and 2-(dimethylhydrazono) -1-phenylethane-1-thione with diazo compounds

Egli, Daniel H.,Linden, Anthony,Heimgartner, Heinz

, p. 86 - 100 (2007)

The reactions of thiobenzamide 8 with diazo compounds proceeded via reactive thiocarbonyl ylides as intermediates, which underwent either a 1,5-dipolar electrocyclization to give the corresponding five membered heterocycles, i.e., 4-amino-4,5-dihydro-1,3-

Addition of trimethylsulfoxoniumylide and methylenetriphenylphosphorane to N2-thioacylamidines

Toure, S. A.,Voglozin, A.,Degny, E.,Danion-Bougot, R.,Danion, D.,et al.

, p. 574 - 579 (2007/10/02)

Trimethylsulfoxonium ylide reacts with 4-dimethylamino-1-thia-3-azabutadienes (N2-thioacylamidines) affording thiazol-2-ines, through a regioselective reaction corresponding to a nucleophilic attack on the amidine group.Thiazoles are obtained b

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