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CAS

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193635-04-0

(1-Trityl-aziridin-2-yl)-methanol, also known as Trityl-aziridine-methanol, is a chemical compound that features a trityl group attached to an aziridine ring. This heterocyclic organic compound is known for its unique structure and reactivity, which arises from the presence of a highly reactive three-membered aziridine ring. The trityl group serves as a common protecting group in organic synthesis, offering stability and protection to the reactive aziridine functionality. (1-Trityl-aziridin-2-yl)-methanol holds promise for use in organic synthesis and as a building block for pharmaceuticals, with potential applications yet to be fully explored through further research and development.

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  • 193635-04-0 Structure

  • Basic information

    1. Product Name: (1-Trityl-aziridin-2-yl)-methanol
    2. Synonyms: (1-Trityl-aziridin-2-yl)-methanol;2-Aziridinemethanol, 1-(triphenylmethyl)-
    3. CAS NO:193635-04-0
    4. Molecular Formula: C22H21NO
    5. Molecular Weight: 315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 193635-04-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1-Trityl-aziridin-2-yl)-methanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-Trityl-aziridin-2-yl)-methanol(193635-04-0)
    11. EPA Substance Registry System: (1-Trityl-aziridin-2-yl)-methanol(193635-04-0)

  • 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: 193635-04-0(Hazardous Substances Data)

193635-04-0 Usage

Uses

Used in Organic Synthesis:
(1-Trityl-aziridin-2-yl)-methanol is used as a building block and reagent in organic synthesis for its unique structure and reactivity. The trityl group provides stability and protection to the aziridine ring, making it suitable for various synthetic pathways and reactions.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1-Trityl-aziridin-2-yl)-methanol is used as a precursor in the synthesis of pharmaceutical compounds. Its potential applications in drug development are attributed to its unique chemical properties, which can be harnessed to create novel therapeutic agents.
Further research and development may reveal additional uses and applications for (1-Trityl-aziridin-2-yl)-methanol across different industries, as its full potential is yet to be discovered.

Check Digit Verification of cas no

The CAS Registry Mumber 193635-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,6,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 193635-04:
(8*1)+(7*9)+(6*3)+(5*6)+(4*3)+(3*5)+(2*0)+(1*4)=150
150 % 10 = 0
So 193635-04-0 is a valid CAS Registry Number.

193635-04-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-tritylaziridin-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 2-Aziridinemethanol,1-(triphenylmethyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:193635-04-0 SDS

193635-04-0Relevant articles and documents

Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds

Molander, Gary A.,Stengel, Peter J.

, p. 8887 - 8912 (2007/10/03)

A convenient method for the reduction of 2-acylaziridines, aziridine-2- carboxylates and aziridine-2-carboxamides is described. The reduction of all of the substrates examined was extremely rapid and highly regioselective, giving rise to β-amino carbonyl compounds. This method appears to be general for all of the classes of aziridines mentioned above, and also tolerates a variety of nitrogen protecting groups.

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