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methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68305-82-8 Structure
  • Basic information

    1. Product Name: methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate
    2. Synonyms: methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate
    3. CAS NO:68305-82-8
    4. Molecular Formula:
    5. Molecular Weight: 285.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68305-82-8.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: methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate(68305-82-8)
    11. EPA Substance Registry System: methyl (S)-4-methyl-2-(phenylsulfonamido)pentanoate(68305-82-8)
  • 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: 68305-82-8(Hazardous Substances Data)

68305-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68305-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,0 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68305-82:
(7*6)+(6*8)+(5*3)+(4*0)+(3*5)+(2*8)+(1*2)=138
138 % 10 = 8
So 68305-82-8 is a valid CAS Registry Number.

68305-82-8Relevant articles and documents

Development of a Direct Photocatalytic C-H Fluorination for the Preparative Synthesis of Odanacatib

Halperin, Shira D.,Kwon, Daniel,Holmes, Michael,Regalado, Erik L.,Campeau, Louis-Charles,Dirocco, Daniel A.,Britton, Robert

, p. 5200 - 5203 (2015)

Late-stage C-H fluorination is an appealing reaction for medicinal chemistry. However, the application of this strategy to process research appears less attractive due to the formation and necessary purification of mixtures of organofluorines. Here we dem

Sulfonamide formation from sodium sulfinates and amines or ammonia under metal-free conditions at ambient temperature

Yang, Kai,Ke, Miaolin,Lin, Yuanguang,Song, Qiuling

supporting information, p. 1395 - 1399 (2015/03/18)

A novel, practical and highly efficient method for the construction of a variety of sulfonamides mediated by I2 was demonstrated. The reaction proceeds readily at room temperature using a variety of sodium sulfinates and amines or ammonia in water in a metal-, base-, ligand-, or additive-free protocol. Primary, secondary and tertiary sulfonamides were obtained in good to excellent yields with a broad range of functional group tolerability. This journal is

Facile ring-opening of azabicyclic [3.1.0]-and [4.1.0]aminocyclopropanes to afford 3-piperidinone and 3-azepinone

Lee, Jisun,Berritt, Simon,Prier, Christopher K.,Joullie, Madeleine M.

supporting information; experimental part, p. 1083 - 1085 (2011/04/22)

Azabicyclic [3.1.0] and [4.1.0] Kulinkovich products underwent a facile reduction/fragmentation to afford a variety of 3-piperidinones and 3-azepinones, respectively, in the presence of catalytic palladium on carbon and formic acid in an atmosphere of hyd

Palladium catalysed queuing processes. Part 2: Termolecular cyclization-anion capture employing carbon monoxide as a relay switch with in situ generated vinylstannanes

Anwar, Usman,Casaschi, Adele,Grigg, Ronald,Sansano, José M

, p. 1361 - 1367 (2007/10/03)

The palladium catalysed termolecular queuing processes involving aryl iodides, carbon monoxide (1 atm) and in situ generated vinylstannanes as terminating agents afford a variety of complex heterocyclic α,β-unsaturated ketones in good yield.

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