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(1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134834-37-0 Structure
  • Basic information

    1. Product Name: (1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine
    2. Synonyms: (1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine
    3. CAS NO:134834-37-0
    4. Molecular Formula:
    5. Molecular Weight: 327.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134834-37-0.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: (1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine(134834-37-0)
    11. EPA Substance Registry System: (1S,2R)-N-C6H5CH2O(CH2)4-N-methylnorephedrine(134834-37-0)
  • 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: 134834-37-0(Hazardous Substances Data)

134834-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134834-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,8,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134834-37:
(8*1)+(7*3)+(6*4)+(5*8)+(4*3)+(3*4)+(2*3)+(1*7)=130
130 % 10 = 0
So 134834-37-0 is a valid CAS Registry Number.

134834-37-0Downstream Products

134834-37-0Relevant articles and documents

New Polymer Bound Chiral Catalyst with Methylene Spacer for the Enantioselective Addition of Diethylzinc to Aldehydes

Soai, Kenso,Watanabe, Masami

, p. 97 - 100 (1991)

Optically active sec-alcohols in good to high e.e.'s were obtained from the enantioselective addition of diethylzinc to both aliphatic and aromatic aldehydes using a polymer attached chiral catalyst with a methylene spacer.

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