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150618-03-4

Nα-Boc 4--L-phenylalanine benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150618-03-4 Structure

  • Basic information

    1. Product Name: Nα-Boc 4--L-phenylalanine benzyl ester
    2. Synonyms: Nα-Boc 4--L-phenylalanine benzyl ester
    3. CAS NO:150618-03-4
    4. Molecular Formula:
    5. Molecular Weight: 541.529
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150618-03-4.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: Nα-Boc 4--L-phenylalanine benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Nα-Boc 4--L-phenylalanine benzyl ester(150618-03-4)
    11. EPA Substance Registry System: Nα-Boc 4--L-phenylalanine benzyl ester(150618-03-4)

  • 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: 150618-03-4(Hazardous Substances Data)

150618-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150618-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,6,1 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150618-03:
(8*1)+(7*5)+(6*0)+(5*6)+(4*1)+(3*8)+(2*0)+(1*3)=104
104 % 10 = 4
So 150618-03-4 is a valid CAS Registry Number.

150618-03-4Relevant articles and documents

Facile syntheses of aryldifluorophosphonate building blocks

Cockerill, G. Stuart,Easterfield, Howard J.,Percy, Jonathan M.

, p. 2601 - 2604 (2007/10/03)

The copper-catalysed zinc phosphonate chemistry described by Yokomatsu and Shibuya can be used directly in the synthesis of phosphotyrosine analogue F2Pmp, and in entering the classical organometallic coupling repertoire via Stille and Suzuki-M

Enantioselective synthesis of N-Boc and N-Fmoc protected diethyl 4-phosphono(difluoromethyl)-L-phenylalanine; agents suitable for the solid-phase synthesis of peptides containing nonhydrolyzable analogues of O-phosphotyrosine

Smyth,Burke Jr.

, p. 551 - 554 (2007/10/02)

Enantioselective convergent syntheses of N-Boc and N-Fmoc protected diethyl 4-phosphono(difluoromethyl)-L-phenylalanine are reported.

Preparation of L-(Phosphonodifluoromethyl) phenylalanine derivatives as non-hydrolyzable mimetics of O-phosphotyrosine

Wrobel, Jay,Dietrich, Arlene

, p. 3543 - 3546 (2007/10/02)

N-t-BOC-L-(Phosphonodifluoromethyl)phenylalanine benzyl ester (1) was prepared in 5 steps from N-t-BOC-L-tyrosine benzyl eser O-triflate (4). Compound 1 was further converted to derivatives 2 and 3 which are potentially suitable for peptide synthesis. Ana

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