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1H-Imidazole-4-methanol, a-ethyl-1-(triphenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62256-51-3

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62256-51-3 Usage

Molecular Structure

1H-Imidazole-4-methanol, a-ethyl-1-(triphenylmethyl)consists of an imidazole ring with a hydroxyl group attached to the fourth carbon atom and an ethyl group connected to the nitrogen atom, along with a triphenylmethyl substituent.

Molecular Complexity

The compound has a complex molecular structure.

Imidazole Ring

The compound contains an imidazole ring.

Hydroxyl Group

The compound has a hydroxyl group attached to the fourth carbon atom.

Ethyl Group

The compound has an ethyl group connected to the nitrogen atom.

Triphenylmethyl Substituent

The compound contains a triphenylmethyl substituent, which is a bulky and highly stable organic group.

Potential Applications

1H-Imidazole-4-methanol, a-ethyl-1-(triphenylmethyl)has potential applications in pharmaceuticals, organic synthesis, and materials science.

Unique Structure and Reactivity

The compound has a unique structure and reactivity.

Biological Activity

The compound may exhibit biological activity.

Research and Development Potential

The compound has the potential for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 62256-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,5 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62256-51:
(7*6)+(6*2)+(5*2)+(4*5)+(3*6)+(2*5)+(1*1)=113
113 % 10 = 3
So 62256-51-3 is a valid CAS Registry Number.

62256-51-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-trityl-1H-imidazol-4-yl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 1-(1-Trityl-1H-imidazol-4-yl)-propan-1-ol

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:62256-51-3 SDS

62256-51-3Relevant academic research and scientific papers

NITROGENATED HETEROCYCLIC COMPOUND

-

, (2015/03/28)

The present invention provides a compound having a PDE2A selective inhibitory action, which is useful as an agent for the prophylaxis or treatment of schizophrenia, Alzheimer's disease and the like. The present invention is a compound represented by the formula (1): wherein each symbol is as described in the specification, or a salt thereof.

Simultaneous deprotection and purification based on ionic resin capture: Application to amide formations and Grignard and Mitsunobu reactions

Meier, Peter,Mueller, Sascha

, p. 2203 - 2207 (2008/03/28)

Products containing Boc- or Tr-protected amines were caught directly out of reaction mixtures by simultaneous cleavage of the protecting group. By releasing the products with ammonia the corresponding free amines were obtained in high yields and purities.

2-OXO-1-PYRROLIDINE DERIVATIVES

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Page/Page column 95, (2008/06/13)

The present invention concerns 2-oxo-1 -pyrrolidine derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals.

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