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(+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121824-05-3 Structure
  • Basic information

    1. Product Name: (+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane
    2. Synonyms: (+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane
    3. CAS NO:121824-05-3
    4. Molecular Formula:
    5. Molecular Weight: 196.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121824-05-3.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(R),S(R)>-p-tolylsulfinyl-2-methyloxirane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane(121824-05-3)
    11. EPA Substance Registry System: (+)-<2(R),S(R)>-p-tolylsulfinyl-2-methyloxirane(121824-05-3)
  • 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: 121824-05-3(Hazardous Substances Data)

121824-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121824-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,2 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 121824-05:
(8*1)+(7*2)+(6*1)+(5*8)+(4*2)+(3*4)+(2*0)+(1*5)=93
93 % 10 = 3
So 121824-05-3 is a valid CAS Registry Number.

121824-05-3Relevant articles and documents

OPTICALLY ACTIVE α-SULFINYL EPOXIDES: PRECURSORS OF CHIRAL FUNCTIONALIZED HOMOALLYLIC ALCOHOLS

Solladie, Guy,Hamdouchi, Chafiq,Vicente, Martina

, p. 5929 - 5932 (1988)

An asymmetric synthesis of chiral functionalized homoallylic alcohols in both configurations is described from the corresponding optically active α-sulfinyl epoxides.

Asymmetric Synthesis of the C-1-C-8 Fragment of Leukotriene B4 and C-11-C-20 Fragments of Leukotriene B4 and 12(S)-Hydroxy-5,8,14(Z), 10(E) Eicosatetraenoic Acid

Solladie, Guy,Hamdouchi, Chafiq,Ziani-Cherif, Chewki

, p. 457 - 469 (2007/10/02)

An asymmetric synthesis of the C-1-C-8 fragment of LTB4 based on the reduction of optically active β-ketosulfoxides is described as well as the asymmetric synthesis of the C-11-C-20 fragments of LTB4 and 12(S)-hydroxy-5,8,14(Z), 10(E

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