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1346899-06-6

C28H41NO2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1346899-06-6 Structure

  • Basic information

    1. Product Name: C28H41NO2S
    2. Synonyms: C28H41NO2S
    3. CAS NO:1346899-06-6
    4. Molecular Formula:
    5. Molecular Weight: 455.705
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1346899-06-6.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: C28H41NO2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C28H41NO2S(1346899-06-6)
    11. EPA Substance Registry System: C28H41NO2S(1346899-06-6)

  • 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: 1346899-06-6(Hazardous Substances Data)

1346899-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346899-06-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,8,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1346899-06:
(9*1)+(8*3)+(7*4)+(6*6)+(5*8)+(4*9)+(3*9)+(2*0)+(1*6)=206
206 % 10 = 6
So 1346899-06-6 is a valid CAS Registry Number.

1346899-06-6Downstream Products

1346899-06-6Relevant articles and documents

Enantioselective bromocyclization of olefins catalyzed by chiral phosphoric acid

Huang, Deshun,Wang, Haining,Xue, Fazhen,Guan, Huan,Li, Lijun,Peng, Xianyou,Shi, Yian

, p. 6350 - 6353 (2011)

A chiral phosphoric acid catalyzed enantioselective bromocyclization of olefins is described. Various cis-, trans-, or trisubstituted ?-hydroxyalkenes and γ-amino-alkenes can cyclize under the reaction conditions to give optically active 2-substituted tetrahydrofurans and tetrahydropyrroles in up to 91% ee.

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