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1358685-46-7

C22H27FN2O4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1358685-46-7 Structure

  • Basic information

    1. Product Name: C22H27FN2O4S
    2. Synonyms: C22H27FN2O4S
    3. CAS NO:1358685-46-7
    4. Molecular Formula:
    5. Molecular Weight: 434.532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1358685-46-7.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: C22H27FN2O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H27FN2O4S(1358685-46-7)
    11. EPA Substance Registry System: C22H27FN2O4S(1358685-46-7)

  • 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: 1358685-46-7(Hazardous Substances Data)

1358685-46-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1358685-46-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,8,6,8 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1358685-46:
(9*1)+(8*3)+(7*5)+(6*8)+(5*6)+(4*8)+(3*5)+(2*4)+(1*6)=207
207 % 10 = 7
So 1358685-46-7 is a valid CAS Registry Number.

1358685-46-7Downstream Products

1358685-46-7Relevant articles and documents

Synthesis of a unique isoindoline/tetrahydroisoquinoline-based tricyclic sultam library utilizing a Heck-aza-Michael strategy

Zang, Qin,Javed, Salim,Porubsky, Patrick,Ullah, Farman,Neuenswander, Benjamin,Lushington, Gerald H.,Basha, Fatima Z.,Organ, Michael G.,Hanson, Paul R.

, p. 211 - 217 (2012/05/19)

The synthesis of a unique isoindoline- and tetrahydroisoquinoline (THIQ)-containing tricyclic sultam library, utilizing a Heck-aza-Michael (HaM) strategy is reported. Both isoindoline and THIQ rings are installed through a Heck reaction on a vinylsulfonamide, followed by one-pot deprotection and intramolecular aza-Michael reaction. Subsequent cyclization with either paraformaldehyde condensation or 1,1′-carbonyldiimidazole coupling generates a variety of tricyclic sultams. Overall, a 160-member library of these sultams, together with their isoindolines/THIQ and secondary sulfonamides precursors, were constructed using this strategy.

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