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trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107832-61-1 Structure
  • Basic information

    1. Product Name: trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane
    2. Synonyms: trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane
    3. CAS NO:107832-61-1
    4. Molecular Formula:
    5. Molecular Weight: 268.571
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107832-61-1.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: trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane(107832-61-1)
    11. EPA Substance Registry System: trimethyl(2-(((trimethylsilyl)methyl)thio)phenyl)silane(107832-61-1)
  • 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: 107832-61-1(Hazardous Substances Data)

107832-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107832-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,3 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107832-61:
(8*1)+(7*0)+(6*7)+(5*8)+(4*3)+(3*2)+(2*6)+(1*1)=121
121 % 10 = 1
So 107832-61-1 is a valid CAS Registry Number.

107832-61-1Downstream Products

107832-61-1Relevant articles and documents

Preparation of Thioanisole Biscarbanion and C-H Lithiation/Annulation Reactions for the Access of Five-Membered Heterocycles

Zhu, Ranran,Liu, Zheyuan,Chen, Jie,Xiong, Xiaoyu,Wang, Yuntao,Huang, Lin,Bai, Jinshan,Dang, Yanfeng,Huang, Jianhui

supporting information, p. 3161 - 3165 (2018/06/11)

The synthesis, isolation, and X-ray structure of a thioanisole-based trilithium complex are reported. On the basis of the double-lithiation strategy, two novel synthetic methodologies have been developed under mild reaction conditions (room temperature): (1) reactions of lithiated thioanisoles with nitriles give benzoisothiazoles via a [3 + 2]-type of approach with two new bond formations and (2) formation of benzothiophenes from thioanisoles and amides through a [4 + 1] pattern forming 4 new chemical bonds.

METALATION REACTIONS. IX. DILITHIATION OF AROMATIC THIOETHERS

Cabiddu, Salvatore,Floris, Constantino,Melis, Stefana

, p. 4625 - 4628 (2007/10/02)

Direct dimetalation of aromatic thioethers gives with good yield the dilithiated species 3, 4, 17, 18, 25, 26.The first four species allowed the simultaneous introduction of an electrophile in the thiomethyl group and in the ring, while the last two species undergo disubstitution in the ring.

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