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1071493-63-4

C10H12F3NO2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1071493-63-4 Structure

  • Basic information

    1. Product Name: C10H12F3NO2S
    2. Synonyms: C10H12F3NO2S
    3. CAS NO:1071493-63-4
    4. Molecular Formula:
    5. Molecular Weight: 267.272
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1071493-63-4.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: C10H12F3NO2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C10H12F3NO2S(1071493-63-4)
    11. EPA Substance Registry System: C10H12F3NO2S(1071493-63-4)

  • 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: 1071493-63-4(Hazardous Substances Data)

1071493-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1071493-63-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,4,9 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1071493-63:
(9*1)+(8*0)+(7*7)+(6*1)+(5*4)+(4*9)+(3*3)+(2*6)+(1*3)=144
144 % 10 = 4
So 1071493-63-4 is a valid CAS Registry Number.

1071493-63-4Relevant articles and documents

Pd(II)-catalyzed o-C-H acetoxylation of phenylalanine and ephedrine derivatives with MeCOOOtBu/Ac2O

Vickers, Chris J.,Mei, Tian-Sheng,Yu, Jin-Quan

supporting information; experimental part, p. 2511 - 2513 (2010/07/06)

Pd(II)-catalyzed ortho C-H acetoxylation of triflate protected phenethyl- and phenpropylamines has been achieved with tert-butyl peroxyacetate as the stoichiometric oxidant and either DMF or CH3CN as the promoter. The reaction was found to tolerate a large variety of functional groups and could be combined with subsequent intramolecular amination to afford functionalized indoline derivatives.

Pd(II)-catalyzed amination of C-H bonds using single-electron or two-electron oxidants

Mei, Tian-Sheng,Wang, Xisheng,Yu, Jin-Quan

supporting information; experimental part, p. 10806 - 10807 (2009/12/04)

(Chemical Equation Presented) Pd(II)-catalyzed intramolecular amination of arenes is developed using either a one- or two-electron oxidant. The reaction protocol tolerates a wide range of deactivating groups including acetyl, cyano, and nitro groups. This catalytic reaction allows expedient syntheses of broadly useful substituted indolines or indoles.

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