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19263-21-9

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19263-21-9 Usage

General Description

Bromoethyltriflate is a chemical compound with the molecular formula C4H5BrO3. It is a colorless to pale yellow liquid that is highly reactive and is commonly used as a reagent in organic synthesis. Bromoethyltriflate is a powerful alkylating agent, meaning it can transfer its ethyl group to other molecules, and is often used in the synthesis of pharmaceuticals and other organic compounds. It is also used as a reagent in the preparation of various functionalized compounds and as a potential precursor for the synthesis of alkylating agents. However, it is important to handle bromoethyltriflate with care, as it is highly toxic and can cause severe skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 19263-21-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19263-21:
(7*1)+(6*9)+(5*2)+(4*6)+(3*3)+(2*2)+(1*1)=109
109 % 10 = 9
So 19263-21-9 is a valid CAS Registry Number.

19263-21-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoethyl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 1-bromo-2-(p-toluenesulfonyloxy)ethane

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:19263-21-9 SDS

19263-21-9Relevant articles and documents

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Kochi,J.K. et al.

, p. 3503 - 3515 (1968)

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LOX INHIBITORS

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Paragraph 00379-00382; 00398, (2020/06/05)

The disclosure relates to compounds of Formula I, or pharmaceutically acceptable salts thereof, Formula (I) as defined herein. Compounds according to Formula I are pharmacologically effective as lysyl oxidase (LOX) inhibitors and are believed to be useful in the treatment of, for instance, cancer.

Alkynyl-substituted heterocyclic compound, preparation method therefor and medical use therefor for effectively treating and/or preventing FGFR-related diseases such as tumors

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Page/Page column 89-90, (2020/02/18)

The present invention relates to an alkynyl-substituted heterocyclic compound serving as an FGFR inhibitor, a preparation method therefor and a medical use therefor. In particular, the present invention relates to a compound represented by the general formula (I) and its pharmaceutically acceptable salt, a pharmaceutical composition including the compound or its pharmaceutically acceptable salt, a method for treating and/or preventing FGFR-related diseases, particularly tumors, by using the compound or its pharmaceutically acceptable salt, and a preparation method of the compound or its pharmaceutically acceptable salt. The present invention also relates to an use of the compound or its pharmaceutically acceptable salt, or an pharmaceutical composition including the compound or its pharmaceutically acceptable salt in the preparation of a drug for treating and/or preventing FGFR-related diseases, particularly tumors, wherein the definition of each substituent in the general formula (I) is the same as that in the specification.

Synthesis, radiolabeling and evaluation of novel amine guanidine derivatives as potential positron emission tomography tracers for the ion channel of the N-methyl-d-aspartate receptor

Klein, Pieter J.,Chomet, Marion,Metaxas, Athanasios,Christiaans, Johannes A.M.,Kooijman, Esther,Schuit, Robert C.,Lammertsma, Adriaan A.,Van Berckel, Bart N.M.,Windhorst, Albert D.

, p. 143 - 160 (2016/05/09)

The N-Methyl-d-Aspartate receptor (NMDAR) is involved in many neurological and psychiatric disorders including Alzheimer's disease and schizophrenia. The aim of this study was to develop a positron emission tomography (PET) ligand to assess the bio-availa

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