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CAS

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1244056-14-1

4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1244056-14-1 Structure

  • Basic information

    1. Product Name: 4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide
    2. Synonyms: 4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide
    3. CAS NO:1244056-14-1
    4. Molecular Formula:
    5. Molecular Weight: 242.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1244056-14-1.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: 4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide(1244056-14-1)
    11. EPA Substance Registry System: 4-(4-nitrophenyl)-5H-[1,2,3]oxathiazole 2,2-dioxide(1244056-14-1)

  • 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: 1244056-14-1(Hazardous Substances Data)

1244056-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1244056-14-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,0,5 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1244056-14:
(9*1)+(8*2)+(7*4)+(6*4)+(5*0)+(4*5)+(3*6)+(2*1)+(1*4)=121
121 % 10 = 1
So 1244056-14-1 is a valid CAS Registry Number.

1244056-14-1Downstream Products

1244056-14-1Relevant articles and documents

Enantioselective synthesis of cyclic sulfamidates by using chiral rhodium-catalyzed asymmetric transfer hydrogenation

Kang, Soyeong,Han, Juae,Lee, Eun Sil,Choi, Eun Bok,Lee, Hyeon-Kyu

supporting information; experimental part, p. 4184 - 4187 (2010/11/19)

Asymmetric transfer hydrogenation (ATH) of cyclic sulfamidate imines 4 and 9, using a HCO2H/Et3N mixture as the hydrogen source and well-defined chiral Rh catalysts (S,S)- or (R,R)-2, CpRhCl(TsDPEN), effectively produces the corresponding cyclic sulfamidates with excellent yields and enantioselectivities at room temperature within 0.5 h. ATH of 4,5-disubstituted imines 9, having preexisting stereogenic centers, is shown to take place with dynamic kinetic resolution.

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