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2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1330147-04-0 Structure
  • Basic information

    1. Product Name: 2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane
    2. Synonyms: 2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane
    3. CAS NO:1330147-04-0
    4. Molecular Formula:
    5. Molecular Weight: 213.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1330147-04-0.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: 2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane(1330147-04-0)
    11. EPA Substance Registry System: 2-deutero-2-(2'-hydroxyphenyl)-1,3-dithiane(1330147-04-0)
  • 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: 1330147-04-0(Hazardous Substances Data)

1330147-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1330147-04-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,1,4 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1330147-04:
(9*1)+(8*3)+(7*3)+(6*0)+(5*1)+(4*4)+(3*7)+(2*0)+(1*4)=100
100 % 10 = 0
So 1330147-04-0 is a valid CAS Registry Number.

1330147-04-0Relevant articles and documents

Rh-Catalyzed domino synthesis of 4-hydroxy-3-methylcoumarins via branch-selective hydroacylation

Rao, Maddali L.N.,Ramakrishna, Boddu S.,Nand, Sachchida

, p. 9275 - 9279 (2019/11/13)

A Rh-catalyzed domino synthesis of 4-hydroxy-3-methylcoumarins via branch-selective hydroacylation of acrylates and acrylamides using salicylaldehydes is described. This protocol under phosphine-free Rh-catalyzed conditions provided 4-hydroxy-3-methylcoum

Mechanistic investigation of the enantioselective intramolecular stetter reaction: Proton transfer is the first irreversible step

Moore, Jennifer L.,Silvestri, Anthony P.,De Alaniz, Javier Read,Dirocco, Daniel A.,Rovis, Tomislav

, p. 1742 - 1745 (2011/06/17)

A study on the mechanism of the asymmetric intramolecular Stetter reaction is reported. This investigation includes the determination of the rate law, kinetic isotope effects, and competition experiments. The reaction was found to be first order in aldehy

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