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CAS

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176848-07-0

methyl 2-benzylsulfanyl-2-fluoroacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 176848-07-0 Structure

  • Basic information

    1. Product Name: methyl 2-benzylsulfanyl-2-fluoroacetate
    2. Synonyms: methyl 2-benzylsulfanyl-2-fluoroacetate
    3. CAS NO:176848-07-0
    4. Molecular Formula:
    5. Molecular Weight: 214.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 176848-07-0.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 2-benzylsulfanyl-2-fluoroacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 2-benzylsulfanyl-2-fluoroacetate(176848-07-0)
    11. EPA Substance Registry System: methyl 2-benzylsulfanyl-2-fluoroacetate(176848-07-0)

  • 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: 176848-07-0(Hazardous Substances Data)

176848-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176848-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,8,4 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 176848-07:
(8*1)+(7*7)+(6*6)+(5*8)+(4*4)+(3*8)+(2*0)+(1*7)=180
180 % 10 = 0
So 176848-07-0 is a valid CAS Registry Number.

176848-07-0Relevant articles and documents

Synthesis of α-fluoro-β-hydroxy alkylsulfanyl esters via a nucleophilic fluorination of sulfides

Jouen,Lemaitre,Lequeux,Pommelet

, p. 10801 - 10810 (1998)

By halogen-exchange reaction using NEt3-3HF as fluoride source, methyl 2-fluoro-2-alkylsulfanyl acetate 3a-d could be obtained in good yields. Their ester enolates reacted with aromatic or aliphatic aldehydes, to lead to methyl α-atkylsulfanyl-

Synthesis of α-fluorinated-α,α-difunctionalized sulfides and sulfones

Jouen,Lasne,Pommelet

, p. 2413 - 2416 (2007/10/03)

The highly functionalized organofluorine compounds 3a-c were prepared from the activated dichlorinated sulfides 2a-c by displacement of a chlorine atom using nucleophilic fluorination agents such as dihydrogenfluoride polymer-supported. Fluorination of sulfoxides 5a-c with diethylaminosulfur trifluoride gives monofluoro sulfides 6a-c, subsequently transformed into α-chloro-α-fluoro sulfides 3a-c and sulfones 7a-c.

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