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1211284-05-7

C13H18FNO2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1211284-05-7 Structure

  • Basic information

    1. Product Name: C13H18FNO2S
    2. Synonyms: C13H18FNO2S
    3. CAS NO:1211284-05-7
    4. Molecular Formula:
    5. Molecular Weight: 271.356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1211284-05-7.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: C13H18FNO2S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H18FNO2S(1211284-05-7)
    11. EPA Substance Registry System: C13H18FNO2S(1211284-05-7)

  • 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: 1211284-05-7(Hazardous Substances Data)

1211284-05-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1211284-05-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,2,8 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1211284-05:
(9*1)+(8*2)+(7*1)+(6*1)+(5*2)+(4*8)+(3*4)+(2*0)+(1*5)=97
97 % 10 = 7
So 1211284-05-7 is a valid CAS Registry Number.

1211284-05-7Downstream Products

1211284-05-7Relevant articles and documents

Highly functional group compatible Rh-catalyzed addition of arylboroxines to activated N-tert-butanesulfinyl ketimines

Jung, Hyung Hoon,Buesking, Andrew W.,Ellman, Jonathan A.

supporting information; experimental part, p. 3912 - 3915 (2011/09/16)

The rhodium-catalyzed addition of readily accessible arylboroxines to N-tert-butanesulfinyl ketimines derived from oxetan-3-one, N-Boc-azetidin-3-one, and isatins proceeds in high yields with excellent functional group compatibility. Moreover, high diastereoselectivities are observed for the additions to the N-sulfinyl ketimines derived from isatins.

Reactions of oxetan-3-tert-butylsulfinimine for the preparation of substituted 3-aminooxetanes

Hamzik, Philip J.,Brubaker, Jason D.

supporting information; experimental part, p. 1116 - 1119 (2010/06/11)

(Figure Presented) The oxetane ring Is useful In drug discovery as a bioisostere for both the geminal dimethyl group and the carbonyl group. A convenient, straightforward approach to access structurally diverse 3-aminooxetanes through the reactivity of oxetan-3-tert-butylsulfinimine and the corresponding sulfinylaziridine Is described.

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