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1587718-03-3

(R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1587718-03-3 Structure

  • Basic information

    1. Product Name: (R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide
    2. Synonyms: (R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide
    3. CAS NO:1587718-03-3
    4. Molecular Formula:
    5. Molecular Weight: 351.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1587718-03-3.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: (R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide(1587718-03-3)
    11. EPA Substance Registry System: (R)-N-(2-iodobenzyl)-N-methyl-t-butanesulfinamide(1587718-03-3)

  • 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: 1587718-03-3(Hazardous Substances Data)

1587718-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1587718-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,7,7,1 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1587718-03:
(9*1)+(8*5)+(7*8)+(6*7)+(5*7)+(4*1)+(3*8)+(2*0)+(1*3)=213
213 % 10 = 3
So 1587718-03-3 is a valid CAS Registry Number.

1587718-03-3Relevant articles and documents

Sulfur-Based Chiral Iodoarenes: An Underexplored Class of Chiral Hypervalent Iodine Reagents

Alharbi, Haifa,Elsherbini, Mohamed,Karam, Fatemah,Osi, Arnaud,Wirth, Thomas

, (2021)

Chiral hypervalent iodine reagents are active players in modern stereoselective organic synthesis. Structurally diverse chiral hypervalent iodine reagents have been synthesised and extensively studied, but hypervalent iodine reagents containing chiral sul

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