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154607-00-8

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154607-00-8 Usage

Description

2-Bromo-5-hydroxybenzoic acid Methyl ester, also known as Methyl 2-Bromo-5-hydroxybenzoate, is an organic compound derived from hydroxybenzoic acid. It is characterized by the presence of a bromine atom at the 2nd position and a hydroxyl group at the 5th position, with a methyl ester functional group. 2-broMo-5-hydroxybenzoic acid Methyl ester exhibits unique chemical properties that make it suitable for various applications in different industries.

Uses

Used in Pharmaceutical Industry:
2-Bromo-5-hydroxybenzoic acid Methyl ester is used as a key intermediate in the synthesis of macrocyclic Mcl-1 inhibitors. These inhibitors are designed for the treatment of multiple myeloma, a type of blood cancer. The compound plays a crucial role in the development of novel therapeutic agents that target the Mcl-1 protein, which is overexpressed in multiple myeloma cells and contributes to the resistance of these cells to apoptosis.
In the pharmaceutical industry, 2-Bromo-5-hydroxybenzoic acid Methyl ester is used as a building block for the creation of macrocyclic Mcl-1 inhibitors. These inhibitors are specifically designed to target and inhibit the Mcl-1 protein, which is overexpressed in multiple myeloma cells and plays a significant role in the resistance of these cells to apoptosis. By inhibiting Mcl-1, these macrocyclic compounds can potentially enhance the effectiveness of current treatments for multiple myeloma and improve patient outcomes.

Check Digit Verification of cas no

The CAS Registry Mumber 154607-00-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,6,0 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 154607-00:
(8*1)+(7*5)+(6*4)+(5*6)+(4*0)+(3*7)+(2*0)+(1*0)=118
118 % 10 = 8
So 154607-00-8 is a valid CAS Registry Number.

154607-00-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-bromo-5-hydroxybenzoate

1.2 Other means of identification

Product number -
Other names methyl 2-bromo-5-hydroxybenzenecarboxylate

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:154607-00-8 SDS

154607-00-8Relevant articles and documents

A Chan-Evans-Lam approach to trisubstituted vinyl ethers

Molder, Bryce A.,Sader, Jonathan K.,Wulff, Jeremy E.

supporting information, p. 9649 - 9653 (2021/12/01)

Trisubstituted vinyl ethers were accessedviaChan-Evans-Lam coupling of vinyl trifluoroborates and primary aliphatic alcohols. This approach complements prior methods that required the use of neat liquid alcohol coupling partners. A palladium-catalyzed redox-relay Heck reaction was used to convert several vinyl ethers into aldehyde-functionalized 1,3-dihydroisobenzofurans.

Concise Synthesis of a Potential 5-Lipoxygenase Activating Protein (FLAP) Inhibitor and Its Analogs through Late-Stage Alkene Dicarbofunctionalization

Kc, Shekhar,Dhungana, Roshan K.,Aryal, Vivek,Giri, Ramesh

, p. 1686 - 1694 (2019/07/04)

We report a five-step synthesis of the biologically important 1,1-diarylalkane 1, a potential 5-lipoxygenase activating protein (FLAP) inhibitor that was synthesized previously in 12 steps. In this synthesis, we apply a three-component alkene dicarbofunct

A pH-sensitive near-infrared fluorescent probe with alkaline p: K a for chronic wound monitoring in diabetic mice

Mai, Hengtang,Wang, Yu,Li, Shuang,Jia, Ruizhen,Li, Sixian,Peng, Qian,Xie, Yan,Hu, Xiang,Wu, Song

supporting information, p. 7374 - 7377 (2019/06/27)

A pH-sensitive near-infrared fluorescent probe with alkaline pKa, AlkaP-1, was developed by incorporating a benzoyl hydrazine group into a cyanine dye. The significant fluorescence changes in the alkaline regions enable the probe to monitor the alkalization process from acute wounds to chronic wounds in diabetic mice.

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