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tert-butyl 5-methoxy-2-(6-((2S,3S)-3-methyl-4-oxo-3-phenyloxetan-2-yl)pyridin-2-yl)-1H-indole-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1426961-82-1 Structure
  • Basic information

    1. Product Name: tert-butyl 5-methoxy-2-(6-((2S,3S)-3-methyl-4-oxo-3-phenyloxetan-2-yl)pyridin-2-yl)-1H-indole-1-carboxylate
    2. Synonyms:
    3. CAS NO:1426961-82-1
    4. Molecular Formula:
    5. Molecular Weight: 484.552
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1426961-82-1.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: tert-butyl 5-methoxy-2-(6-((2S,3S)-3-methyl-4-oxo-3-phenyloxetan-2-yl)pyridin-2-yl)-1H-indole-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 5-methoxy-2-(6-((2S,3S)-3-methyl-4-oxo-3-phenyloxetan-2-yl)pyridin-2-yl)-1H-indole-1-carboxylate(1426961-82-1)
    11. EPA Substance Registry System: tert-butyl 5-methoxy-2-(6-((2S,3S)-3-methyl-4-oxo-3-phenyloxetan-2-yl)pyridin-2-yl)-1H-indole-1-carboxylate(1426961-82-1)
  • 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: 1426961-82-1(Hazardous Substances Data)

1426961-82-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1426961-82-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,6,9,6 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1426961-82:
(9*1)+(8*4)+(7*2)+(6*6)+(5*9)+(4*6)+(3*1)+(2*8)+(1*2)=181
181 % 10 = 1
So 1426961-82-1 is a valid CAS Registry Number.

1426961-82-1Downstream Products

1426961-82-1Relevant articles and documents

NHC-promoted asymmetric β-lactone formation from arylalkylketenes and electron-deficient benzaldehydes or pyridinecarboxaldehydes

Douglas, James,Taylor, James E.,Churchill, Gwydion,Slawin, Alexandra M. Z.,Smith, Andrew D.

, p. 3925 - 3938 (2013/06/26)

A chiral NHC catalyzes the asymmetric formal [2 + 2] cycloaddition of alkylarylketenes with both electron-deficient benzaldehydes and 2- and 4-pyridinecarboxaldehydes to generate stereodefined β-lactones. In the benzaldehyde series, optimal product diastereo- and enantiocontrol is observed using 2-nitrobenzaldehyde (up to 93:7 dr (syn:anti) and 93% ee). Substituted 2- and 4-pyridinecarboxaldehydes are also tolerated in this process, generating the corresponding β-lactones in good yield and enantioselectivity, although the diastereocontrol in these processes is highly dependent upon the aldehyde substitution. These processes are readily scalable, allowing multigram quantities of the β-lactone products to be prepared. Derivatization of these products, either through ring opening into the corresponding stereodefined β-hydroxy and β-amino acid derivatives without loss of stereochemical integrity or via cross-coupling, is demonstrated.

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