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154049-34-0

methyl (2R,5R)-5-benzoyloxy-N-methoxycarbonyl-piperidine-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 154049-34-0 Structure

  • Basic information

    1. Product Name: methyl (2R,5R)-5-benzoyloxy-N-methoxycarbonyl-piperidine-2-carboxylate
    2. Synonyms:
    3. CAS NO:154049-34-0
    4. Molecular Formula:
    5. Molecular Weight: 321.33
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154049-34-0.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: methyl (2R,5R)-5-benzoyloxy-N-methoxycarbonyl-piperidine-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2R,5R)-5-benzoyloxy-N-methoxycarbonyl-piperidine-2-carboxylate(154049-34-0)
    11. EPA Substance Registry System: methyl (2R,5R)-5-benzoyloxy-N-methoxycarbonyl-piperidine-2-carboxylate(154049-34-0)

  • 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: 154049-34-0(Hazardous Substances Data)

154049-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154049-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,4 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 154049-34:
(8*1)+(7*5)+(6*4)+(5*0)+(4*4)+(3*9)+(2*3)+(1*4)=120
120 % 10 = 0
So 154049-34-0 is a valid CAS Registry Number.

154049-34-0Downstream Products

154049-34-0Relevant articles and documents

Synthesis of 2S,5S- and 2R,5S-5-hydroxypipecolic acid via amide-methylenation of S-5-hydroxy-2-piperidone with dimethyltitanocene

Herdeis,Heller

, p. 2085 - 2094 (1993)

A route to 2S,5S-hydroxypipecolic acid is presented, starting with the enantiopure 5S-5-hydroxy-piperidone 7. The key step of this reaction sequence is the chemoselective methylation of the amide carbonyl group of 8 with dimethyltitanocene 9 to 10. The tr

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