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143060-93-9

(R)-β,β-diphenyl-α-alanine hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143060-93-9 Structure

  • Basic information

    1. Product Name: (R)-β,β-diphenyl-α-alanine hydrochloride
    2. Synonyms: (R)-β,β-diphenyl-α-alanine hydrochloride
    3. CAS NO:143060-93-9
    4. Molecular Formula:
    5. Molecular Weight: 277.751
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143060-93-9.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: (R)-β,β-diphenyl-α-alanine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-β,β-diphenyl-α-alanine hydrochloride(143060-93-9)
    11. EPA Substance Registry System: (R)-β,β-diphenyl-α-alanine hydrochloride(143060-93-9)

  • 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: 143060-93-9(Hazardous Substances Data)

143060-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143060-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,0,6 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143060-93:
(8*1)+(7*4)+(6*3)+(5*0)+(4*6)+(3*0)+(2*9)+(1*3)=99
99 % 10 = 9
So 143060-93-9 is a valid CAS Registry Number.

143060-93-9Relevant articles and documents

Cobalt-mediated alkylation of (4R) and (4S)-3-acetoacetyl-4-benzyloxazolidin-2-ones. Preparation of enantiopure diphenylmethyl-, 9-fluorenyl-, and (1-adamantyl)glycines

Galvez, Nicanor,Moreno-Manas, Marcial,Vallribera, Adelina,Molins, Elies,Cabrero, Araceli

, p. 6197 - 6200 (2007/10/03)

The Co(II) complexes of (4R) and (4S)-3-acetoacetyl-4-benzyloxazolidin-2-ones are alkylated diastereoselectively with diphenylmethyl, 9-fluorenyl, and 1-adamantyl bromide. The resulting products are converted into enantiopure α-substituted glycines. Similar results are obtained by alkylation of the free acetoacetyloxazolidinones under Co(II)-catalysis.

Stereocontrolled Conversion of L-Serine into a Series of Valuable Unnatural α-Amino Acids

Koskinen, Ari M. P.,Hassila, Heikki,Myllymaeki, Vesa T.,Rissanen, Karl

, p. 5619 - 5622 (2007/10/02)

Stereocontrolled synthesis of (2R,3S)- and (2R,3R)-phenylserine, (R)-3,3-diphenylserine and (R)-3,3-diphenylalanine are described.

Process for the preparation of D(-) and L(+)-3,3-diphenylalanine and D(-) and L(+)-substituted 3,3-diphenylalanines and derivatives thereof

-

, (2008/06/13)

A process for the preparation of D(-) and L(+)-3,3-diphenylalanine and D(-) and L(+)-substituted 3,3-diphenylalanines is described where N-protected DL-3,3-diphenylalanine or N-protected-DL-substituted 3,3-diphenylalanine are treated with (-)cinchonidine and the resulting salt resolved into the desired enantiomers, as well as derivatives thereof and valuable intermediates used in the process.

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