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1206669-38-6

1-(1,5-diphenyl-2-pentyn-1-yl)piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1206669-38-6 Structure

  • Basic information

    1. Product Name: 1-(1,5-diphenyl-2-pentyn-1-yl)piperidine
    2. Synonyms: 1-(1,5-diphenyl-2-pentyn-1-yl)piperidine
    3. CAS NO:1206669-38-6
    4. Molecular Formula:
    5. Molecular Weight: 303.447
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206669-38-6.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: 1-(1,5-diphenyl-2-pentyn-1-yl)piperidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(1,5-diphenyl-2-pentyn-1-yl)piperidine(1206669-38-6)
    11. EPA Substance Registry System: 1-(1,5-diphenyl-2-pentyn-1-yl)piperidine(1206669-38-6)

  • 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: 1206669-38-6(Hazardous Substances Data)

1206669-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206669-38-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,6,6 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1206669-38:
(9*1)+(8*2)+(7*0)+(6*6)+(5*6)+(4*6)+(3*9)+(2*3)+(1*8)=156
156 % 10 = 6
So 1206669-38-6 is a valid CAS Registry Number.

1206669-38-6Downstream Products

1206669-38-6Relevant articles and documents

Highly efficient three-component coupling reaction catalysed by atomically precise ligand-protected Au38(SC2H4Ph)24 nanoclusters

Li, Qi,Das, Anindita,Wang, Shuxin,Chen, Yuxiang,Jin, Rongchao

, p. 14298 - 14301 (2016)

The catalytic potential of atomically precise quantum-sized gold nanoclusters (Au38(SC2H4Ph)24) is explored for the three-component coupling of an aldehyde, an alkyne and an amine to synthesize propargylamines.

Synthesis of N,N-disubstituted 3-amino-1,4-diynes and 3-amino-1-ynes by addition of alkynyldimethylaluminum reagents to N,N-disubstituted formamides and N,O-acetals

Korbad, Balaji L.,Lee, Sang-Hyeup

, p. 5089 - 5095 (2014/08/18)

A wide range of alkynyldimethylaluminum reagents, which were derived from terminal alkynes and trimethylaluminum, underwent a double addition to N,N-disubstituted formamides and their acetals to provide the corresponding N,N-disubstituted 3-amino-1,4-diynes in moderate to excellent yields. Also, these reagents smoothly underwent the addition to N,O-acetals to give the corresponding N,N-disubstituted 3-amino-1-ynes in excellent yields.

N-heterocyclic carbene (NHC)-copper(I) complexes as catalysts for A 3 reactions

Chen, Ming-Tsz,Navarro, Oscar

, p. 1190 - 1192 (2013/07/05)

The use of easily synthesized NHC-Cu(I) complexes for the preparation of a variety of propargylamines through an A3 coupling scheme is described. Georg Thieme Verlag Stuttgart New York.

Well-defined (N-heterocyclic carbene)-Ag(i) complexes as catalysts for A3 reactions

Chen, Ming-Tsz,Landers, Brant,Navarro, Oscar

supporting information; experimental part, p. 2206 - 2208 (2012/04/10)

The use of well-defined (N-heterocyclic carbene)-Ag(i) complexes for the A3 reaction allows for the coupling of unactivated aldehydes at room temperature and very short reaction times. The Royal Society of Chemistry 2012.

Impregnated copper on magnetite: An efficient and green catalyst for the multicomponent preparation of propargylamines under solvent free conditions

Aliaga, Maria J.,Ramon, Diego J.,Yus, Miguel

scheme or table, p. 43 - 46 (2010/05/19)

Impregnated copper on magnetite is a versatile, inexpensive and simple catalyst for the selective multicomponent reaction of terminal alkynes, aldehydes and secondary amines to give the corresponding propargylamines with excellent yields. The catalyst can

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