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131654-56-3

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131654-56-3 Usage

General Description

2-Bromomethylthiazole is a chemical compound with the molecular formula C4H4BrNS. It is a thiazole derivative that contains a bromomethyl group attached to the thiazole ring. 2-Bromomethylthiazole is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It can undergo various chemical reactions, such as nucleophilic substitution and cross-coupling reactions, to form different compounds with diverse biological activities. 2-Bromomethylthiazole is a versatile building block in organic synthesis and is used in the production of biologically active molecules, making it an important chemical in the pharmaceutical and agricultural industries.

Check Digit Verification of cas no

The CAS Registry Mumber 131654-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,6,5 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 131654-56:
(8*1)+(7*3)+(6*1)+(5*6)+(4*5)+(3*4)+(2*5)+(1*6)=113
113 % 10 = 3
So 131654-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H4BrNS/c5-3-4-6-1-2-7-4/h1-2H,3H2

131654-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(bromomethyl)-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2-BROMOMETHYL-THIAZOLE

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:131654-56-3 SDS

131654-56-3Relevant articles and documents

Cyclams with Ambidentate Methylthiazolyl Pendants for Stable, Inert, and Selective Cu(II) Coordination

Rodríguez-Rodríguez, Aurora,Halime, Zakaria,Lima, Luís M.P.,Beyler, Maryline,Deniaud, David,Le Poul, Nicolas,Delgado, Rita,Platas-Iglesias, Carlos,Patinec, Véronique,Tripier, Rapha?l

, p. 619 - 632 (2016)

Aiming to develop new copper chelates for application in nuclear medicine we report two new chelators, te1th and te2th, based on a cyclam backbone mono-N- or di-N1,N8-functionalized by methylthiazolyl arms. The acid-base properties of both ligands were investigated as well as their coordination chemistry, especially with Cu2+, when possible in aqueous solution and in the solid state. Single-crystal X-ray diffraction structures of complexes were determined. Stability constants of the copper(II) and zinc(II) complexes showed that the complexes of both ligands with Cu2+ are thermodynamically very stable, and they exhibit an important selectivity for Cu2+ over Zn2+. The kinetic inertness in acidic medium of both copper(II) complexes was evaluated revealing a quite good resistance to dissociation (the half-life times of complexes with te1th and te2th are 50.8 and 5.8 min, respectively, in 5 M HCl and 30 °C). The coordination geometry of the metal center in the complexes was established in aqueous solution based on UV-visible, electron paramagnetic resonance (EPR) spectroscopy, DFT studies, and NMR by using the zinc(II) complex analogues. The [Cu(te1th)]2+ and [Cu(te2th)]2+ complexes adopt trans-I and trans-III configurations both in the solid state and in solution, while the [Zn(te2th)]2+ complex crystallizes as the cis-V isomer but exists in solution as a mixture of trans-III and cis-V forms. Cyclic voltammetry experiments in acetonitrile point to a relatively easy reduction of [Cu(te2th)]2+ in acetonitrile solution (Epc = -0.41 V vs NHE), but the reduced complex does not undergo dissociation in the time scale of our electrochemical experiments. The results obtained in these studies revealed that despite the limited solubility of its copper(II) chelate, te2th is an attractive chelator for Cu2+ that provides a fast complexation process while forming a complex with a rather high thermodynamic stability and kinetic inertness with respect to dissociation even upon electrochemical reduction.

Hetero-aromatic compound and its use in medicine

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Paragraph 0883; 0898-0900, (2019/07/04)

The invention provides a hetero-aromatic compound or a stereisomer, geometric isomer, tautomer, despinner, nitrogen oxide, hydrate, solvate, metabolite, metabolism precursor and pharmaceutically acceptable salt or prodrug thereof, which is used for treating proliferative diseases. The invention also discloses a pharmaceutical composition containing the compound and an application of the compound or pharmaceutical composition thereof in preparation of a medicine for treating proliferative diseases.

COMPOUNDS THAT INHIBIT MCL-1 PROTEIN

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Page/Page column 1027; 1028, (2017/09/15)

Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.

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