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CAS

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127086-92-4

(4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127086-92-4 Structure

  • Basic information

    1. Product Name: (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan
    2. Synonyms: (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan
    3. CAS NO:127086-92-4
    4. Molecular Formula:
    5. Molecular Weight: 355.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127086-92-4.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: (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan(127086-92-4)
    11. EPA Substance Registry System: (4S,5S)-5-<(benzyloxycarbonyl)(methyl)amino>-2,2-dimethyl-4-phenyl-1,3-dioxan(127086-92-4)

  • 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: 127086-92-4(Hazardous Substances Data)

127086-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127086-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,0,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127086-92:
(8*1)+(7*2)+(6*7)+(5*0)+(4*8)+(3*6)+(2*9)+(1*2)=134
134 % 10 = 4
So 127086-92-4 is a valid CAS Registry Number.

127086-92-4Downstream Products

127086-92-4Relevant articles and documents

Enantioselective Preparation of (2R)- and (2S)-Azetidine-2-carboxylic Acids

Wessig, Pablo,Schwarz, Jutta

, p. 1803 - 1814 (2007/10/03)

The enantiomerically pure amino ketones 13 and 31 were prepared starting from the commercially available amino diol 9 and D-serine (21), respectively. Irradiation afforded highly functionalized azetidinols 15 and 33 in a fully stereoselective manner and i

Oxazolophanes as masked cyclopeptide alkaloid equivalents: Cyclic peptide chemistry without peptide couplings

Lipshutz, Bruce H.,Huff, Bret E.,McCarthy, Keith E.,Miller, Todd A.,Jaweed Mukarram,Siahaan, Teruna J.,Vaccaro, Wayne D.,Webb, Hugh,Falick, Arnold M.

, p. 7032 - 7041 (2007/10/02)

Synthetic studies on the preparation of heteroatom-substituted, novel [3.3]oxazolophanes as precursors to the 14-membered ring system characteristic of the cyclopeptide alkaloids are reported. Simpler model systems are discussed, as is the successful form

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