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Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 783297-54-1 Structure
  • Basic information

    1. Product Name: Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI)
    2. Synonyms: Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI)
    3. CAS NO:783297-54-1
    4. Molecular Formula: C10H21N
    5. Molecular Weight: 155.28044
    6. EINECS: N/A
    7. Product Categories: METHYL
    8. Mol File: 783297-54-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI)(783297-54-1)
    11. EPA Substance Registry System: Piperidine, 2-butyl-6-methyl-, (2R,6R)-rel- (9CI)(783297-54-1)
  • 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: 783297-54-1(Hazardous Substances Data)

783297-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 783297-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,2,9 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 783297-54:
(8*7)+(7*8)+(6*3)+(5*2)+(4*9)+(3*7)+(2*5)+(1*4)=211
211 % 10 = 1
So 783297-54-1 is a valid CAS Registry Number.

783297-54-1Downstream Products

783297-54-1Relevant articles and documents

Regioselective generation of iminium cation by PET processes: Its in situ trapping by intramolecular nucleophiles and synthesis of some biologically active heterocycles

Pandey,Kumaraswamy,Yella Reddy

, p. 8295 - 8308 (2007/10/02)

Efficient, mild and direct route for regiospecific iminium cation is developed by sequential two electron oxidation of several N-alkylated tertiary amines by photoinduced electron transfer processes. The regiospecificity of iminium cation arises from the deprotonation step of amine radical cation to generate α-amino radical which depends on the stereoelectronic factor subject to kinetic acidity of amine radical cation. Iminium cation is efficiently trapped in situ by internal nucleophiles to give cyclic compounds 14-18 and 22a-c. Stereoselective synthesis of cis α,α'-dialkylated piperidines and pyrrolidines 30a-c is achieved by nucleophilic opening of tetrahydro-1,3-oxazines 22a-c.

Regiocontrolled set promoted photocyclisation of 2-alkyl-1-piperidine and pyrrolidine propanols: Stereoselective synthesis of cis-α,α′-dialkyl piperidines and pyrrolidines via tetrahydro-1,3-oxazines

Pandey, Ganesh,Yella Reddy,Bhalerao

, p. 5147 - 5150 (2007/10/02)

Photocyclisation of amino alcohols (1a-c) to (4a-c) via insitu generated iminium cation by photoinduced SET reaction and their utility in the stereoselective synthesis of cis-α-α′-dialkyl piperidines and pyrrolidines is described.

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