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3-(benzyl(methyl)amino)-2-hydroxy-2-(hydroxymethyl)propyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1206202-06-3 Structure
  • Basic information

    1. Product Name: 3-(benzyl(methyl)amino)-2-hydroxy-2-(hydroxymethyl)propyl acetate
    2. Synonyms:
    3. CAS NO:1206202-06-3
    4. Molecular Formula:
    5. Molecular Weight: 267.325
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206202-06-3.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: 3-(benzyl(methyl)amino)-2-hydroxy-2-(hydroxymethyl)propyl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(benzyl(methyl)amino)-2-hydroxy-2-(hydroxymethyl)propyl acetate(1206202-06-3)
    11. EPA Substance Registry System: 3-(benzyl(methyl)amino)-2-hydroxy-2-(hydroxymethyl)propyl acetate(1206202-06-3)
  • 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: 1206202-06-3(Hazardous Substances Data)

1206202-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206202-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,2,0 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1206202-06:
(9*1)+(8*2)+(7*0)+(6*6)+(5*2)+(4*0)+(3*2)+(2*0)+(1*6)=83
83 % 10 = 3
So 1206202-06-3 is a valid CAS Registry Number.

1206202-06-3Upstream product

1206202-06-3Downstream Products

1206202-06-3Relevant articles and documents

Towards a chemo-enzymatic method for the asymmetric synthesis of β-amino tertiary alcohols

March-Cortijos, Andrea,Snape, Timothy J.

, p. 5163 - 5165 (2009)

The synthesis of a number of β-amino tertiary alcohols has been achieved via ring-opening of an unsymmetrical epoxide with primary and secondary amines. The results revealed that primary amines give symmetrical triol products following an undesired acyl m

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