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  • 1437311-30-2 Structure
  • Basic information

    1. Product Name: C22H37NS
    2. Synonyms: C22H37NS
    3. CAS NO:1437311-30-2
    4. Molecular Formula:
    5. Molecular Weight: 347.608
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1437311-30-2.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: C22H37NS(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H37NS(1437311-30-2)
    11. EPA Substance Registry System: C22H37NS(1437311-30-2)
  • 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: 1437311-30-2(Hazardous Substances Data)

1437311-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1437311-30-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,7,3,1 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1437311-30:
(9*1)+(8*4)+(7*3)+(6*7)+(5*3)+(4*1)+(3*1)+(2*3)+(1*0)=132
132 % 10 = 2
So 1437311-30-2 is a valid CAS Registry Number.

1437311-30-2Downstream Products

1437311-30-2Relevant articles and documents

Pd-catalyzed α-arylation of thioamides

Yu, Hailei,Liu, Xuliang,Ding, Lei,Yang, Qin,Rong, Bin,Gao, Ang,Zhao, Baoguo,Yang, Haifeng

, p. 3060 - 3062 (2013)

Thioamides are unique and versatile synthetic building blocks with S, N, and α-C three adjacent nucleophile centers, however, they are rarely used as carbon nucleophiles for transition-metal-catalyzed C-C coupling reactions. This Letter describes the first Pd-catalyzed α-arylation of thioamides and demonstrated the feasibility of the application of thioamides in coupling chemistry. By the coupling process, a variety of α-arylated thioamides were prepared in moderate to good yields under mild reaction conditions, which provides an alternative way to access functionalized thioamides as well as a new synthetic transformation for thioamides. High chemoselectivity for thioamide over amide was observed in the reaction.

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