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4-(Chloromethyl)-1-trityl-1H-imidazole is a chemical compound that belongs to the class of organic compounds known as trityls. These compounds contain a trityl moiety, which consists of a phenyl group substituted with three methyl groups. Specifically, in 4-(chloromethyl)-1-trityl-1H-imidazole, a trityl group is connected to an imidazole ring, which is a five-membered ring with two nitrogen atoms. The chloromethyl group is connected to the imidazole ring as well. The presence of chloromethyl group imparts reactivity to the compound, making it a valuable compound in chemical synthesis processes. Like many organic compounds, it is typically used in laboratory settings and is handled following safety procedures due to its reactivity and potential toxicity.

103057-10-9

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103057-10-9 Usage

Uses

Used in Chemical Synthesis:
4-(Chloromethyl)-1-trityl-1H-imidazole is used as a reagent for chemical synthesis processes due to its reactivity. The chloromethyl group allows for various chemical reactions, making it a versatile compound in the synthesis of other organic compounds.
Used in Laboratory Research:
4-(Chloromethyl)-1-trityl-1H-imidazole is used as a research compound in academic and industrial laboratories. Its unique structure and reactivity make it a valuable tool for studying chemical reactions and exploring new synthetic pathways.
Used in Pharmaceutical Development:
4-(Chloromethyl)-1-trityl-1H-imidazole is used as a building block in the development of new pharmaceuticals. Its reactivity and structural features can be exploited to create novel drug candidates with potential therapeutic applications.
Used in Material Science:
4-(Chloromethyl)-1-trityl-1H-imidazole is used as a component in the synthesis of new materials with specific properties. Its reactivity can be utilized to create materials with tailored characteristics for various applications, such as in electronics or advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 103057-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,0,5 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103057-10:
(8*1)+(7*0)+(6*3)+(5*0)+(4*5)+(3*7)+(2*1)+(1*0)=69
69 % 10 = 9
So 103057-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H19ClN2/c24-16-22-17-26(18-25-22)23(19-10-4-1-5-11-19,20-12-6-2-7-13-20)21-14-8-3-9-15-21/h1-15,17-18H,16H2

103057-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Chloromethyl)-1-trityl-1H-imidazole

1.2 Other means of identification

Product number -
Other names 4-(chloromethyl)-1-tritylimidazole

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:103057-10-9 SDS

103057-10-9Relevant 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

, (2021)

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

ANDROGEN RECEPTOR MODULATORS AND METHODS FOR THEIR USE

-

, (2020/05/06)

The present invention relates to compounds of formula (I)-(VI) and/or (A)-(H-I), or any subgenera thereof, or a pharmaceutically acceptable salt, tautomer or stereoisomer. The compounds of the present disclosure are useful in modulating androgen receptor activity and for treating cancer including prostate cancer.

HETEROARYL RHEB INHIBITORS AND USES THEREOF

-

, (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

-

, (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

Synthesis and evaluation of potent, highly-selective, 3-aryl-piperazinone inhibitors of protein geranylgeranyltransferase-I

Peng, Hairuo,Carrico, Dora,Thai, Van,Blaskovich, Michelle,Bucher, Cynthia,Pusateri, Erin E.,Sebti, Said M.,Hamilton, Andrew D.

, p. 1768 - 1784 (2008/02/05)

A series of compounds based on the carboxyl-terminal CAAL sequence of PGGTase-I substrates was designed and synthesized. Using piperazin-2-one as a semi-rigid scaffold, we have introduced critical pharmacophores in a well-defined arrangement to mimic the CAAL sequence. High potency and exceptional selectivity were obtained for inhibition of PGGTase-I with structures such as 45 and 70. Potency of this series of GGTIs was dependent on the presence of an l-leucine residue with a free carboxyl terminus, as well as an S configuration of the 3-aryl group. The selectivity was significantly enhanced by 5-methyl substitution on the imidazole ring and fluorine substitution on the 3-aryl group. Modification of the 6-position of the piperazinone scaffold was found to be unfavorable. Compounds 44 and 69, the corresponding methyl esters of 45 and 70, were found to selectively block processing of Rap1A by PGGTase-I in whole cells with IC50 values of 0.4 M and 0.7 M respectively. The Royal Society of Chemistry 2006.

Design, synthesis, and pharmacological evaluation of new farnesyl protein transferase inhibitors

Houssin, Raymond,Pommery, Jean,Salaün, Marie-Catherine,Deweer, Sophie,Goossens, Jean-Fran?ois,Chavatte, Philippe,Hénichart, Jean-Pierre

, p. 533 - 536 (2007/10/03)

New CA1A2X peptidomimetics are described as Ras farnesyl transferase inhibitors (FTIs). They include cysteine and methionine as mimetics of the C-terminus sequence of farnesylated proteins. Furthermore, cysteine was replaced by heter

INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE

-

, (2008/06/13)

The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting farnesyl-protein transferase and the farnesylation of the oncogene protein Ras

INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE

-

, (2008/06/13)

The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invent

4-METHOXY-5-METHYL-PYRAN-3-OL NATURAL PRODUCTS AND DERIVATIVES THEREOF

-

, (2008/06/13)

Novel antibiotic substances, including novel natural products, having the general formula wherein R1 and R2 are as defined herein, are disclosed. These compounds have been found to be cytochrome P450 inhibitors.

5-(HETEROCYCLYLALKANOYL)AMINO-4-HYDROXYPENTANAMIDES

-

, (2008/06/13)

This invention concerns novel nitrogen derivatives of the formula I STR1 (and their pharmaceutically-acceptable salts), together with pharmaceutical compositions containing them. The nitrogen derivatives are inhibitors of the catalytic action of renin. Th

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