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904682-06-0

methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 904682-06-0 Structure

  • Basic information

    1. Product Name: methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate
    2. Synonyms: methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate
    3. CAS NO:904682-06-0
    4. Molecular Formula:
    5. Molecular Weight: 388.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 904682-06-0.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: methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate(904682-06-0)
    11. EPA Substance Registry System: methyl (2R)-(-)-2-{[(4-bromophenyl)sulfonyl]amino}-3-(2-furyl)propanoate(904682-06-0)

  • 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: 904682-06-0(Hazardous Substances Data)

904682-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 904682-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,4,6,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 904682-06:
(8*9)+(7*0)+(6*4)+(5*6)+(4*8)+(3*2)+(2*0)+(1*6)=170
170 % 10 = 0
So 904682-06-0 is a valid CAS Registry Number.

904682-06-0Relevant 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

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