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127759-47-1

(R)-2-FURANALANINE 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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  • 127759-47-1 Structure

  • Basic information

    1. Product Name: (R)-2-FURANALANINE METHYL ESTER
    2. Synonyms: (R)-2-FURANALANINE METHYL ESTER
    3. CAS NO:127759-47-1
    4. Molecular Formula: C8H11NO3
    5. Molecular Weight: 169.179
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127759-47-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (R)-2-FURANALANINE METHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-FURANALANINE METHYL ESTER(127759-47-1)
    11. EPA Substance Registry System: (R)-2-FURANALANINE METHYL ESTER(127759-47-1)

  • 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: 127759-47-1(Hazardous Substances Data)

127759-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127759-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,5 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127759-47:
(8*1)+(7*2)+(6*7)+(5*7)+(4*5)+(3*9)+(2*4)+(1*7)=161
161 % 10 = 1
So 127759-47-1 is a valid CAS Registry Number.

127759-47-1Relevant articles and documents

Asymmetric rhodium-catalyzed hydrogenation meets gold-catalyzed cyclization: Enantioselective synthesis of 8-hydroxytetrahydroisoquinolines

Hashmi, A. Stephen K.,Haufe, Patrick,Schmid, Christoph,Nass, Andreas Rivas,Frey, Wolfgang

, p. 5376 - 5382 (2008/02/13)

Different furyl-substituted (Z)-dehydroamino acid derivatives were hydrogenated with the rhodium/Mandyphos(OMe)-system to give enantiomeric excesses between 80 and 98%. The absolute configuration of the newly formed stereogenic center was determined by an

Stereoselective synthesis of 3-heteroaromatic-substituted alanines

Croce, Piero Dalla,La Rosa, Concetta,Pizzatti, Enrica

, p. 2635 - 2642 (2007/10/03)

An asymmetric synthesis of (R)-3-heterocyclic-substituted alanines starting from (2S)-(+)-2,5-dihydro-3,6-dimethoxy-2-isopropylpyrazine (Schollkopf reagent) and heteroaromatic halogenomethyl derivatives via hydrolysis of intermediate adducts is reported.

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