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CAS

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63769-00-6

L-Tyrosine, O-(phenylmethyl)-, trifluoroacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63769-00-6 Structure

  • Basic information

    1. Product Name: L-Tyrosine, O-(phenylmethyl)-, trifluoroacetate
    2. Synonyms:
    3. CAS NO:63769-00-6
    4. Molecular Formula: C16H17NO3.C2HF3O2
    5. Molecular Weight: 385.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63769-00-6.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: L-Tyrosine, O-(phenylmethyl)-, trifluoroacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Tyrosine, O-(phenylmethyl)-, trifluoroacetate(63769-00-6)
    11. EPA Substance Registry System: L-Tyrosine, O-(phenylmethyl)-, trifluoroacetate(63769-00-6)

  • 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: 63769-00-6(Hazardous Substances Data)

63769-00-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63769-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63769-00:
(7*6)+(6*3)+(5*7)+(4*6)+(3*9)+(2*0)+(1*0)=146
146 % 10 = 6
So 63769-00-6 is a valid CAS Registry Number.

63769-00-6Relevant articles and documents

Facile synthesis of α-hydroxy carboxylic acids from the corresponding α-amino acids

Stuhr-Hansen, Nicolai,Padrah, Shahrokh,Str?mgaard, Kristian

, p. 4149 - 4151 (2014)

An effective and improved procedure is developed for the synthesis of α-hydroxy carboxylic acids by treatment of the corresponding protonated α-amino acid with tert-butyl nitrite in 1,4-dioxane-water. The amino moiety must be protonated and located α to a carboxylic acid function in order to undergo initial diazotization and successive hydroxylation, since neither β-amino acids nor acid derivatives such as esters and amides undergo hydroxylations. The method is successfully applied for the synthesis of 18 proteinogenic amino acids.

FKBP BINDING COMPOSITION AND PHARMACEUTICAL USE THEREOF

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Page/Page column 89-90, (2010/02/15)

A composition for binding FKBP proteins is disclosed, along with a method of treating conditions associated with neuronal degeneration, wherein said composition comprises a compound of Formula (I), wherein, R, R1, R2, R3 a

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