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methyl 3-amino-3-deoxy-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37098-46-7 Structure
  • Basic information

    1. Product Name: methyl 3-amino-3-deoxy-β-D-galactopyranoside
    2. Synonyms: methyl 3-amino-3-deoxy-β-D-galactopyranoside
    3. CAS NO:37098-46-7
    4. Molecular Formula:
    5. Molecular Weight: 193.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37098-46-7.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 3-amino-3-deoxy-β-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-amino-3-deoxy-β-D-galactopyranoside(37098-46-7)
    11. EPA Substance Registry System: methyl 3-amino-3-deoxy-β-D-galactopyranoside(37098-46-7)
  • 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: 37098-46-7(Hazardous Substances Data)

37098-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37098-46-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,9 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37098-46:
(7*3)+(6*7)+(5*0)+(4*9)+(3*8)+(2*4)+(1*6)=137
137 % 10 = 7
So 37098-46-7 is a valid CAS Registry Number.

37098-46-7Downstream Products

37098-46-7Relevant articles and documents

Arynes in the Monoarylation of Unprotected Carbohydrate Amines

Pal, Kumar Bhaskar,Mahanti, Mukul,Nilsson, Ulf J.

, p. 616 - 619 (2018)

A CsF-mediated method has been developed for the N-arylation of amino sugars that affords good to excellent yields of arylated products under mild conditions involving the in situ generation of arynes. The reaction conditions tolerate a variety of common carbohydrate protecting groups and also performs exceptionally well on unprotected amino sugar derivatives. The reactions are scalable in moderate to good yields with broad scope.

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