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1027143-47-0

3-(4-benzyloxy-3-formyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1027143-47-0 Structure

  • Basic information

    1. Product Name: 3-(4-benzyloxy-3-formyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester
    2. Synonyms:
    3. CAS NO:1027143-47-0
    4. Molecular Formula:
    5. Molecular Weight: 429.47
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1027143-47-0.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: 3-(4-benzyloxy-3-formyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-benzyloxy-3-formyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester(1027143-47-0)
    11. EPA Substance Registry System: 3-(4-benzyloxy-3-formyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester(1027143-47-0)

  • 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: 1027143-47-0(Hazardous Substances Data)

1027143-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027143-47-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,1,4 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1027143-47:
(9*1)+(8*0)+(7*2)+(6*7)+(5*1)+(4*4)+(3*3)+(2*4)+(1*7)=110
110 % 10 = 0
So 1027143-47-0 is a valid CAS Registry Number.

1027143-47-0Relevant articles and documents

A convenient preparation of selectively protected L-Dopa derivatives from 3-iodo-L-tyrosine

Morera,Ortar

, p. 2115 - 2122 (2007/10/03)

Palladium-catalyzed hydroformylation of 3-iodo-L-tyrosine derivatives la,b followed by protection of the free phenol as its benzyl ether and Baeyer-Villiger oxidation of the 3-formyl group provided the desired L-Dopa derivatives 4b,c in 71 and 68% overall

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