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1-(4-(methylthio)phenyl)pyrrolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21608-10-6 Structure
  • Basic information

    1. Product Name: 1-(4-(methylthio)phenyl)pyrrolidine
    2. Synonyms: 1-(4-(methylthio)phenyl)pyrrolidine
    3. CAS NO:21608-10-6
    4. Molecular Formula:
    5. Molecular Weight: 193.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21608-10-6.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: 1-(4-(methylthio)phenyl)pyrrolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-(methylthio)phenyl)pyrrolidine(21608-10-6)
    11. EPA Substance Registry System: 1-(4-(methylthio)phenyl)pyrrolidine(21608-10-6)
  • 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: 21608-10-6(Hazardous Substances Data)

21608-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21608-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,0 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21608-10:
(7*2)+(6*1)+(5*6)+(4*0)+(3*8)+(2*1)+(1*0)=76
76 % 10 = 6
So 21608-10-6 is a valid CAS Registry Number.

21608-10-6Downstream Products

21608-10-6Relevant articles and documents

Visible-Light-Mediated C(sp3)–H Thiocarbonylation for Thiolactam Preparation with Potassium Sulfide

Tan, Wei,Wang, Cuihong,Jiang, Xuefeng

, p. 1234 - 1238 (2019)

We report herein a protocol for thiolactam preparation with potassium sulfide via visible-light-mediated C(sp3)–H thiocarbonylation, in which polysulfide dianions and radical anions generated from potassium sulfide were the key active species. A variety of thiolactams were straightforward established under mild conditions. Moreover, it was successfully applied to structural modification of tetrahydroberberine.

CuI/DMPAO-catalyzed N-arylation of acyclic secondary amines

Zhang, Yu,Yang, Xinye,Yao, Qizheng,Ma, Dawei

supporting information; experimental part, p. 3056 - 3059 (2012/07/28)

DMPAO has been found to be a powerful ligand to enable copper-catalyzed coupling of aryl halides with aliphatic acyclic secondary amines take place under relatively mild conditions, and coupling of aryl halides with primary amines and cyclic secondary amines proceeds at low catalyst loading.

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