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1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 485817-52-5 Structure
  • Basic information

    1. Product Name: 1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione
    2. Synonyms: 1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione
    3. CAS NO:485817-52-5
    4. Molecular Formula:
    5. Molecular Weight: 502.588
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 485817-52-5.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: 1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione(485817-52-5)
    11. EPA Substance Registry System: 1-p-methoxybenzyl-3-tert-butoxycarbonylamino-5-(p-toluenesulfonyl)-piperidine-2,6-dione(485817-52-5)
  • 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: 485817-52-5(Hazardous Substances Data)

485817-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 485817-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,5,8,1 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 485817-52:
(8*4)+(7*8)+(6*5)+(5*8)+(4*1)+(3*7)+(2*5)+(1*2)=195
195 % 10 = 5
So 485817-52-5 is a valid CAS Registry Number.

485817-52-5Relevant articles and documents

A synthesis of thalidomide

Chang, Meng-Yang,Chang, Chung-Ho,Chen, Shui-Tein,Chang, Nein-Chen

, p. 383 - 385 (2002)

A synthesis of racemic thalidomide (1) was described and the important formal [3+3] cycloaddition strategy was a key step. The total yield of thalidomide (1) was 18% in five steps from known 3.

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