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1311377-57-7

N-(4-methoxybenzyl)non-5-yn-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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  • 1311377-57-7 Structure

  • Basic information

    1. Product Name: N-(4-methoxybenzyl)non-5-yn-4-amine
    2. Synonyms: N-(4-methoxybenzyl)non-5-yn-4-amine
    3. CAS NO:1311377-57-7
    4. Molecular Formula:
    5. Molecular Weight: 259.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1311377-57-7.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-(4-methoxybenzyl)non-5-yn-4-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-methoxybenzyl)non-5-yn-4-amine(1311377-57-7)
    11. EPA Substance Registry System: N-(4-methoxybenzyl)non-5-yn-4-amine(1311377-57-7)

  • 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: 1311377-57-7(Hazardous Substances Data)

1311377-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311377-57-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,3,7 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1311377-57:
(9*1)+(8*3)+(7*1)+(6*1)+(5*3)+(4*7)+(3*7)+(2*5)+(1*7)=127
127 % 10 = 7
So 1311377-57-7 is a valid CAS Registry Number.

1311377-57-7Relevant articles and documents

Diversity-oriented synthesis of 1,3-benzodiazepines

Wang, Gaigai,Liu, Chao,Li, Binbin,Wang, Yingchun,Van Hecke, Kristof,Van der Eycken, Erik V.,Pereshivko, Olga P.,Peshkov, Vsevolod A.

, p. 6372 - 6380 (2017)

A concise assembly of the 1,3-benzodiazepine core from A3-coupling-derived propargylamines and ortho-bromophenylisocyanates is described. The developed synthetic sequence involves the addition of propargylamine to isocyanate followed by palladium-catalyzed intramolecular alkyne hydroarylation that could be accomplished in a stepwise or one-pot manner.

Copper-Catalyzed Reaction of Secondary Propargylamines with Ethyl Buta-2,3-dienoate for the Synthesis of 1,6-Dihydropyridines

Liu, Chao,Wang, Gaigai,Wang, Yuqing,Pereshivko, Olga P.,Peshkov, Vsevolod A.

supporting information, p. 1981 - 1985 (2018/12/05)

A copper(I) bromide-catalyzed reaction of A3-coupling-derived propargylamines with ethyl buta-2,3-dienoate for the fast assembly of a 1,6-dihydropyridine core is described. The developed protocol was tested on a variety of secondary propargylamines and the possibility of a one-pot synthesis of 1,6-dihydropyridine through the A3-coupling and subsequent ethyl buta-2,3-dienoate incorporation was investigated.

Tetrasubstituted 2-imidazolones via ag(I)-catalyzed cycloisomerization of propargylic ureas

Peshkov, Vsevolod A.,Pereshivko, Olga P.,Sharma, Sweta,Meganathan, Thirumal,Parmar, Virinder S.,Ermolat'Ev, Denis S.,Van Der Eycken, Erik V.

experimental part, p. 5867 - 5872 (2011/09/14)

A one-pot protocol based on a Ag(I)-catalyzed cycloisomerization of propargylic ureas, derived from secondary propargylamines and isocyanates, was developed for the generation of the 2-imidazolone core.

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