957207-09-9

Basic information

• Product Name: (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL
• Synonyms: (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL;4-Bromo-3-(trifluoromethyl)benzyl alcohol;4-Bromo-3-(trifluoromethyl)benzylalcohol98%;Benzenemethanol, 4-bromo-3-(trifluoromethyl)-
• CAS NO: 957207-09-9
• Molecular Formula: C₈H₆BrF₃O
• Molecular Weight: 255.03
• Mol File: 957207-09-9.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL(957207-09-9)
• EPA Substance Registry System: (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL(957207-09-9)

Safety Data

• Hazardous Substances Data: 957207-09-9(Hazardous Substances Data)

Usage

Description

(4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL, with the molecular formula C8H6BrF3O, is a white crystalline powder that serves as a versatile chemical compound. It has a molecular weight of 249.03 g/mol and is utilized in a range of applications across chemical and pharmaceutical industries.
Used in Pharmaceutical Industry:
(4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new medications.
Used in Agrochemical Industry:
(4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL is used as an intermediate in the synthesis of agrochemicals, playing a role in the creation of substances that help protect crops and enhance agricultural productivity.
Used in Organic Chemistry:
(4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL is used as a building block for the production of other organic compounds, highlighting its importance in the synthesis of various chemical entities.
Safety Note:
(4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL can be hazardous if not handled properly, and it is crucial to take necessary precautions when working with this chemical compound.

Upstream product

• 107317-58-8 4-bromo-3-trifluoromethylbenzoic acid methyl ester 
• 957207-03-3 methyl (3,4-bis(trifluoromethyl)benzoate) 
• 161622-14-6 4-bromo-3-(trifluoromethyl)benzoic acid 
• 364-11-4 1-bromo-4-iodo-2-(trifluoromethyl)benzene 
• 393-36-2 4-bromo-3-(trifluoromethyl)aniline 

Downstream Products

• 1159512-68-1 1-bromo-4-(bromomethyl)-2-(trifluoromethyl)benzene 
• 1243245-72-8 4-bromo-3-(trifluoromethyl)benzyl methanesulfonate 
• 34328-47-7 4-dibromo-3-(trifluoromethyl)benzaldehyde 
• 800379-62-8 O-(4-cyclohexyl-3-trifluoromethyl-benzyl)-hydroxylamine 

Relevant articles and documents

Intermediate of siponimod and synthesis method thereof

The invention relates to a novel intermediate compound (a compound as shown in a formula 2A) of siponimod, a synthesis method of the novel intermediate compound, and a method for synthesizing siponimod by adopting the compound as shown in the formula 2A. Specifically, 3-trifluoromethyl-4-halogenated benzoic acid or 3-trifluoromethyl-4-halogenated toluene is taken as an initial raw material and is subjected to reduction, bromination, coupling, substitution and reduction to obtain a compound as shown in a formula 2A, and R is Boc or Ac.

SELECTIVE FLUORESCENT PROBE FOR ALDEHYDE DEHYDROGENASE

High aldehyde dehydrogenase 1A1 (ALDH1A1) activity has emerged as a reliable marker for the identification of both normal and cancer stem cells. Herein, is presented AlDeSense, a turn-on green fluorescent probe for aldehyde dehydrogenase 1A1 (ALDH1A1) and Ctrl-AlDeSense, a matching non-responsive reagent. AlDeSense exhibits a 20-fold fluorescent enhancement when treated with ALDH1A1. Through the application of surface marker antibody staining, tumorsphere assays, and assessment of tumorigenicity, the disclosed results show that cells exhibiting high AlDeSense signal intensity have properties of cancer stem cells. Herein, is also reported the development of a red congener, red-AlDeSense. Importantly, red-AlDeSense represents one of only a few examples of a turn-on sensor in the red region using the d-PeT quenching mechanism.

Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).