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33769-07-2

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33769-07-2 Usage

General Description

1-TRITYL-1H-IMIDAZOLE-4-METHANOL is a chemical compound that belongs to the class of imidazole derivatives. It is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various drugs and bioactive molecules. 1-TRITYL-1H-IMIDAZOLE-4-METHANOL is known for its ability to act as a versatile reagent in the formation of carbon-carbon and carbon-nitrogen bonds, making it a valuable tool in the production of complex organic compounds. Additionally, 1-TRITYL-1H-IMIDAZOLE-4-METHANOL has been studied for its potential therapeutic applications in the treatment of various diseases and disorders, highlighting its significance in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 33769-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33769-07:
(7*3)+(6*3)+(5*7)+(4*6)+(3*9)+(2*0)+(1*7)=132
132 % 10 = 2
So 33769-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C23H20N2O/c26-17-22-16-25(18-24-22)23(19-10-4-1-5-11-19,20-12-6-2-7-13-20)21-14-8-3-9-15-21/h1-16,18,26H,17H2

33769-07-2SDS

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-Trityl-1H-imidazole-4-methanol

1.2 Other means of identification

Product number -
Other names (1-tritylimidazol-4-yl)methanol

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:33769-07-2 SDS

33769-07-2Relevant articles and documents

Targeting GRP receptor: Design, synthesis and preliminary biological characterization of new non-peptide antagonists of bombesin

Palmioli, Alessandro,Nicolini, Gabriella,Tripodi, Farida,Orsato, Alexandre,Ceresa, Cecilia,Donzelli, Elisabetta,Arici, Martina,Coccetti, Paola,Rocchetti, Marcella,La Ferla, Barbara,Airoldi, Cristina

supporting information, (2021/02/27)

We report the rational design, synthesis, and in vitro preliminary evaluation of a new small library of non-peptide ligands of Gastrin Releasing Peptide Receptor (GRP-R), able to antagonize its natural ligand bombesin (BN) in the nanomolar range of concen

HETEROARYL RHEB INHIBITORS AND USES THEREOF

-

Paragraph 00401, (2018/11/10)

The present invention provides compounds, compositions thereof, and methods of using the same. Compositions comprising a compound of this invention or a pharmaceutically acceptable derivative thereof and a pharmaceutically acceptable carrier, adjuvant, or vehicle. The amount of the compound in compositions of this invention is such that it is effective to measurably inhibit Rheb, in a biological sample or in a patient.

Synthesis method of calmodulin inhibitor for treating brain-derived diseases

-

Paragraph 0033; 0034; 0035, (2017/08/29)

The invention discloses a synthesis method of a calmodulin inhibitor for treating brain-derived diseases and belongs to the technical field of synthesis of chemicals. The technical scheme is characterized in that a synthetic route of the synthesis method

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