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153482-01-0

(-)-Benzyl (2S)-cis-2-formyl-6-methylpiperidine-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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  • 153482-01-0 Structure

  • Basic information

    1. Product Name: (-)-Benzyl (2S)-cis-2-formyl-6-methylpiperidine-1-carboxylate
    2. Synonyms:
    3. CAS NO:153482-01-0
    4. Molecular Formula:
    5. Molecular Weight: 261.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153482-01-0.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: (-)-Benzyl (2S)-cis-2-formyl-6-methylpiperidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-Benzyl (2S)-cis-2-formyl-6-methylpiperidine-1-carboxylate(153482-01-0)
    11. EPA Substance Registry System: (-)-Benzyl (2S)-cis-2-formyl-6-methylpiperidine-1-carboxylate(153482-01-0)

  • 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: 153482-01-0(Hazardous Substances Data)

153482-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153482-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,8 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 153482-01:
(8*1)+(7*5)+(6*3)+(5*4)+(4*8)+(3*2)+(2*0)+(1*1)=120
120 % 10 = 0
So 153482-01-0 is a valid CAS Registry Number.

153482-01-0Downstream Products

153482-01-0Relevant articles and documents

A SHORT, PRACTICAL SYNTHESIS OF THE ANT VENOM ALKALOID, THREE (3R,5S,8aS)-3-ALKYL-5-METHYLINDOLIZIDINES

Takahata, Hiroki,Bandoh, Hiroshi,Momose, Takefumi

, p. 11205 - 11212 (1993)

A short, practical and diastereoselective method for preparing the ant venom alkaloid, three (3R,5S,8aS)-3-alkyl-5-methylindolizidines (1-3), has been developed.The stereoselective intramolecular amidomercuration of the N-alkenylurethane 4 followed by oxidative demercuration provides the piperidine alcohol cis-6 as a major product.Thereafter, oxidation of cis-6 followed by the Horner-Emmons elongation of the ring appendages affords the enones 8, 10, and 11, which are stereoselectively converted into 1, 2, and 3, respectively, by catalytic hydrogenation.

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