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1355952-03-2

4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1355952-03-2 Structure

  • Basic information

    1. Product Name: 4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole
    2. Synonyms: 4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole
    3. CAS NO:1355952-03-2
    4. Molecular Formula:
    5. Molecular Weight: 508.552
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1355952-03-2.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: 4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole(1355952-03-2)
    11. EPA Substance Registry System: 4-bromo-3-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-tosyl-1H-indole(1355952-03-2)

  • 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: 1355952-03-2(Hazardous Substances Data)

1355952-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1355952-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,9,5 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1355952-03:
(9*1)+(8*3)+(7*5)+(6*5)+(5*9)+(4*5)+(3*2)+(2*0)+(1*3)=172
172 % 10 = 2
So 1355952-03-2 is a valid CAS Registry Number.

1355952-03-2Relevant articles and documents

Asymmetric Synthesis of Lysergic Acid via an Intramolecular (3+2) Dipolar Cycloaddition/Ring-Expansion Sequence

Rathnayake, Upendra,Garner, Philip

, p. 6756 - 6759 (2021)

An effective, potentially scalable asymmetric synthesis of lysergic acid, a core component of the ergot alkaloid family, is reported. The synthesis features the strategic combination of an intramolecular azomethine ylide cycloaddition and Cossy-Charette r

Concise synthesis of (R)-aurantioclavine

Ikota, Hideo,Tsukano, Chihiro,Takemoto, Yoshiji

, p. 621 - 631 (2019/07/31)

A synthetic route to (r)-aurantioclavine has been established using a six-step transformation without toxic metal reagents. This synthetic route is useful because it is not only a short-step synthesis but is applicable to gram-scale synthesis of a protect

Enantioselective total syntheses of communesins A and B

Zuo, Zhiwei,Ma, Dawei

, p. 12008 - 12011 (2012/02/02)

As easy as A, B: The first total syntheses of (-)-communesins A and B (see picture) were achieved, which featured the formation of their spiro-fused indoline part through an intramolecular oxidative coupling and of their A ring through a cascade reaction.

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