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957207-09-9

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957207-09-9 Usage

General Description

(4-Bromo-3-trifluoromethyl-phenyl)-methanol is a chemical compound with the molecular formula C8H6BrF3O. It is a white crystalline powder with a molecular weight of 249.03 g/mol. (4-BROMO-3-TRIFLUOROMETHYL-PHENYL)-METHANOL is used in various chemical and pharmaceutical applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block for the production of other organic compounds. (4-Bromo-3-trifluoromethyl-phenyl)-methanol can be hazardous if not handled properly, and precautions should be taken when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 957207-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,2,0 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 957207-09:
(8*9)+(7*5)+(6*7)+(5*2)+(4*0)+(3*7)+(2*0)+(1*9)=189
189 % 10 = 9
So 957207-09-9 is a valid CAS Registry Number.

957207-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Bromo-3-(trifluoromethyl)phenyl)methanol

1.2 Other means of identification

Product number -
Other names [4-Bromo-3-(trifluoromethyl)phenyl]methanol

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:957207-09-9 SDS

957207-09-9Relevant articles and documents

AROMATIC RING DERIVATIVE AS IMMUNOREGULATION AND PREPARATION METHOD AND APPLICATION OF AROMATIC RING DERIVATIVE

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Paragraph 0335-0336, (2021/10/15)

Relating to a compound represented by formula (I) and a pharmaceutically acceptable salt of the compound, and an application of the compound as an S1P1 agonist.

SELECTIVE FLUORESCENT PROBE FOR ALDEHYDE DEHYDROGENASE

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Paragraph 0260, (2020/07/14)

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

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Paragraph 0386-0387, (2018/10/21)

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”).

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