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CAS

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287728-33-0

(S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 287728-33-0 Structure

  • Basic information

    1. Product Name: (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol
    2. Synonyms: (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol
    3. CAS NO:287728-33-0
    4. Molecular Formula:
    5. Molecular Weight: 473.644
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 287728-33-0.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: (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol(287728-33-0)
    11. EPA Substance Registry System: (S)-4-phthalimido-2-(tert-butyldiphenylsilyl)oxy-1-butanol(287728-33-0)

  • 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: 287728-33-0(Hazardous Substances Data)

287728-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 287728-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,7,7,2 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 287728-33:
(8*2)+(7*8)+(6*7)+(5*7)+(4*2)+(3*8)+(2*3)+(1*3)=190
190 % 10 = 0
So 287728-33-0 is a valid CAS Registry Number.

287728-33-0Downstream Products

287728-33-0Relevant articles and documents

Stereoselective tetrapyrido[2,1-a]isoindolone synthesis via carbanionic and radical intermediates: a model study for the Tacaman alkaloid D/E ring fusion.

Hunter, Roger,Richards, Philip

, p. 2348 - 2356 (2007/10/03)

Cyclization under both radical and carbanionic conditions of N-substituted 3-phenylsulfanylisoindolin-1-one 14 containing a chiral N-tether incorporating an enoate ester as the acceptor leads to tetrahydropyrido[2,1-a]isoindolones stereoselectively. The m

Stereoselective tetrahydropyrido[2,1-a]isoindolone synthesis via carbanionic and radical intermediates: A model study for the Tacaman alkaloid D/E ring fusion

Hunter, Roger,Richards, Philip

, p. 3755 - 3758 (2007/10/03)

Stereoselective cyclisation of malic acid-derived α-sulfanyllactam (1) via radical and carbanionic intermediates affords stereo-defined tetrahydropyrido[2,1-a]isoindolones as model compounds for the D/E cis-ring fusion of the Tacaman indole alkaloid skele

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