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2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1355024-93-9 Structure
  • Basic information

    1. Product Name: 2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol
    2. Synonyms: 2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol
    3. CAS NO:1355024-93-9
    4. Molecular Formula:
    5. Molecular Weight: 227.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1355024-93-9.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: 2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol(1355024-93-9)
    11. EPA Substance Registry System: 2-(aminomethyl)-3,4,5-trimethoxyphenylmethanol(1355024-93-9)
  • 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: 1355024-93-9(Hazardous Substances Data)

1355024-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1355024-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,0,2 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1355024-93:
(9*1)+(8*3)+(7*5)+(6*5)+(5*0)+(4*2)+(3*4)+(2*9)+(1*3)=139
139 % 10 = 9
So 1355024-93-9 is a valid CAS Registry Number.

1355024-93-9Relevant articles and documents

Diversity-oriented synthesis of polycyclic diazinic scaffolds

Gigant, Nicolas,Claveau, Elise,Bouyssou, Pascal,Gillaizeau, Isabelle

supporting information; experimental part, p. 844 - 847 (2012/03/26)

An efficient and versatile synthesis of a polycyclic diazinic system starting from oxazine has been developed using a two-step Michael/retro Michael and cyclization sequence. The substrates were synthesized with good to high yields giving rapid access to molecular diversity.

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