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CAS

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367967-67-7

N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine 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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  • 367967-67-7 Structure

  • Basic information

    1. Product Name: N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine methyl ester
    2. Synonyms: N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine methyl ester
    3. CAS NO:367967-67-7
    4. Molecular Formula:
    5. Molecular Weight: 401.459
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 367967-67-7.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: N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine methyl ester(367967-67-7)
    11. EPA Substance Registry System: N-[(1,1-dimethylethoxy)carbonyl]-3-hydroxy-O-(phenylmethyl)-L-tyrosine methyl ester(367967-67-7)

  • 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: 367967-67-7(Hazardous Substances Data)

367967-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 367967-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,7,9,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 367967-67:
(8*3)+(7*6)+(6*7)+(5*9)+(4*6)+(3*7)+(2*6)+(1*7)=217
217 % 10 = 7
So 367967-67-7 is a valid CAS Registry Number.

367967-67-7Relevant articles and documents

AMINO ACID DERIVATIVES

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Page/Page column 17-18, (2009/03/07)

Compounds of formula (I) or formula (11) have dopaminergic activity: wherein: R1 is a carboxyl, carboxyl ester, or carboxamide group; R2 is a group - C(=O)-NR3R4, or -S(=O)2-NR3R4; R3 and R4 are independently selected from hydrogen,optionally substituted C1-C6 alkyl, (C1-C5 fluoroalky1)-CH2-, -Q, and -CH2Q, wherein Q is an optionally substituted monocyclic carbocyclic or heterocyclic ring of (3) to (6) ring atoms; or R3 and R4 together with the nitrogen to which they are attached form an optionally substituted monocyclic cycloalkyl or non-aromatic heterocyclic ring of (3) to (8) ring atoms; R5 is hydrogen, or a natural or non-natural alpha amino acid residue linked via a peptide bond; R6 is hydrogen or a group R7C(=O)-; and R7 is C1- C6 alkyl, C1-C6 fluoroalkyl or cyclopropyl

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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