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4-tert-butyliminomethyl-2,2,5,5-tetramethyl-3-imidazoline-1-oxyl, also known as 4-TBIM, is a free radical compound characterized by its unique chemical structure. It consists of an imidazoline ring with a tert-butyl group attached to the nitrogen atom, and a methyl group on the imino carbon. The molecule also features four methyl groups on the imidazoline ring, contributing to its stability. 4-TBIM is a stable free radical, meaning it has an unpaired electron, which is responsible for its unique properties and potential applications in various fields, such as materials science, chemistry, and medicine. Its free radical nature allows it to participate in redox reactions and interact with other molecules, making it a subject of interest for researchers studying radical chemistry and its implications.

1973-36-0

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1973-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1973-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1973-36:
(6*1)+(5*9)+(4*7)+(3*3)+(2*3)+(1*6)=100
100 % 10 = 0
So 1973-36-0 is a valid CAS Registry Number.

1973-36-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-TERT-BUTYLIMINOMETHYL-2,2,5,5-TETRAMETH YL-3-IMIDAZOLINE-1-OXYL,FREE RADICAL

1.2 Other means of identification

Product number -
Other names 4-TERT-BUTYLIMINOMETHYL-2,2,5,5-TETRAMETHYL-3-IMIDAZOLINE-1-OXYL

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:1973-36-0 SDS

1973-36-0Downstream Products

1973-36-0Relevant academic research and scientific papers

Mixed hydride reduction of steroidal diastereomeric oxathiolanes

Shafiullah,Ali, H.,Ogura, H.,Takayanagi, H.

, p. 112 - 116 (2007/10/02)

Mixed hydride reduction of diastereomeric steroidal oxathiolanes such as (6S)-6,6-oxyethylenethio-5α-cholestane 1 and (6R)-6,6-oxyethylenethio-5α-cholestane 4 and their corresponding 3β-chloro and 3β-acetoxy 2-3 an 5-6 analogues was carried out.The hydroxy products obtained were acetylated.The structures of the compounds obtained were established on the basis of their analytical and spectral data.Schemes 1 and 2 explain their formation.

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