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855749-11-0

N-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 855749-11-0 Structure

  • Basic information

    1. Product Name: N-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine
    2. Synonyms: N-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine
    3. CAS NO:855749-11-0
    4. Molecular Formula:
    5. Molecular Weight: 421.519
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 855749-11-0.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-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine(855749-11-0)
    11. EPA Substance Registry System: N-ethynyl-2-(2-(naphthalen-3-yl)ethynyl)-N-tosylbenzenamine(855749-11-0)

  • 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: 855749-11-0(Hazardous Substances Data)

855749-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855749-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,7,4 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 855749-11:
(8*8)+(7*5)+(6*5)+(5*7)+(4*4)+(3*9)+(2*1)+(1*1)=210
210 % 10 = 0
So 855749-11-0 is a valid CAS Registry Number.

855749-11-0Relevant articles and documents

Synthesis of carbazoles by dehydro Diels-Alder reactions of ynamides

Martínez-Esperón, M. Fernanda,Rodríguez, David,Castedo, Luis,Saá, Carlos

, p. 3674 - 3686 (2008/09/19)

A new approach to carbazoles and benzannulated carbazoles by means of intramolecular dehydro Diels-Alder of ynamides is reported. N-(o-Ethynyl)aryl ynamides and N-(o-ethynyl) arylynamides were prepared in a few steps starting from o-iodoaniline. Thermal c

Coupling and cycloaddition of ynamides: Homo- and Negishi coupling of tosylynamides and intramolecular [4 + 2] cycloaddition of N-(o-ethynyl)phenyl ynamides and arylynamides

Martínez-Esperón, María Fernanda,Rodríguez, David,Castedo, Luis,Saá, Carlos

, p. 3843 - 3855 (2007/10/03)

N,N′-aryl- and N,N′-alkyl-buta-1,3-diyne-1,4-ditosylamides have been synthesized for the first time, in good to excellent yields, by copper-catalyzed dimerization of the corresponding N-aryl or N-alkyl tosylynamides. Negishi coupling of N-ethynylzinc tosy

Synthesis of carbazoles from ynamides by intramolecular dehydro Diels-Alder reactions

Martinez-Esperon, Maria Fernanda,Rodriguez, David,Castedo, Luis,Saa, Carlos

, p. 2213 - 2216 (2007/10/03)

(Chemical Equation Presented) A new approach to carbazoles and benzannulated carbazoles by means of intramolecular dehydro Diels-Alder reactions of ynamides is reported. By using this approach, carbazoles and benzo[b]-, tetrahydrobenzo[b]-, naphtho[1,2-b]

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