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CAS

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54429-89-9

N-benzyl-3-oxypyridinium betaine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 54429-89-9 Structure

  • Basic information

    1. Product Name: N-benzyl-3-oxypyridinium betaine
    2. Synonyms: N-benzyl-3-oxypyridinium betaine
    3. CAS NO:54429-89-9
    4. Molecular Formula:
    5. Molecular Weight: 185.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54429-89-9.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-benzyl-3-oxypyridinium betaine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-3-oxypyridinium betaine(54429-89-9)
    11. EPA Substance Registry System: N-benzyl-3-oxypyridinium betaine(54429-89-9)

  • 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: 54429-89-9(Hazardous Substances Data)

54429-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54429-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54429-89:
(7*5)+(6*4)+(5*4)+(4*2)+(3*9)+(2*8)+(1*9)=139
139 % 10 = 9
So 54429-89-9 is a valid CAS Registry Number.

54429-89-9Relevant articles and documents

Solid-phase synthesis of functionalized tropane derivatives via 1,3-dipolar cycloaddition

Caix-Haumesser, Sandrine,Hanna, Issam,Lallemand, Jean-Yves,Peyronel, Jean-Fran?ois

, p. 3721 - 3723 (2001)

1,3-Dipolar cycloaddition of 3-oxidopyridinium betaine to activated olefins on solid-phase leads to resin-bound 8-azabicyclo[3.2.1]octenones which undergo further transformations such as 1,4-addition of nucleophiles. Cleavage of benzyl linker is achieved

Aryne cycloaddition with 3-oxidopyridinium species

Ren, Hailong,Wu, Chunrui,Ding, Xiuxiu,Chen, Xiaoge,Shi, Feng

supporting information, p. 8975 - 8984,10 (2012/12/12)

The [3 + 2] cycloaddition of arynes with 3-oxidopyridinium species is examined using the Kobayashi benzyne precursor. The reaction affords a bicyclo[3.2.1] skeleton under mild conditions. A [7 + 2] cycloaddition mode with a subsequent pyridine ring-opening event has also been observed.

Structure of the Calystegines: New alkaloids of the nortropane family

Ducrot,Lallemand

, p. 3879 - 3882 (2007/10/02)

Three new alkaloids have been isolated from Calystegia sepium; their structures have been established from their 1H and 13C N.M.R. spectra, and confirmed by the synthesis of model compounds.

1,3-Dipolar Character of Six-membered Aromatic Rings. Part 56. The Cycloadditions of Acetylenes and 3-Oxidopyridinium Betaines

Ishag, Christina Y.,Fisher, Keith J.,Ibrahim, Badr Eldin,Iskander, George M.,Katritzky, Alan R.

, p. 917 - 920 (2007/10/02)

Cycloaddition of dimethyl acetylenedicarboxylate with a variety of 1-substituted 3-oxidopyridinium betaines yields novel furan cycloadducts.Methyl phenylpropiolate reacts similarly with the activated 1--3-oxidopyridinium betai

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