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191602-42-3

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191602-42-3 Usage

Description

2-Bromo-1-isopropoxy-4-nitrobenzene is a chemical compound with the molecular formula C10H12BrNO3. It is a nitrobenzene derivative, characterized by the presence of a bromine atom and an isopropoxy group attached to the benzene ring. This yellow solid has a melting point of 103-104°C and is insoluble in water but soluble in organic solvents. Due to its potential health and environmental hazards, it is classified as a hazardous chemical and requires careful handling.

Uses

Used in Pharmaceutical Industry:
2-Bromo-1-isopropoxy-4-nitrobenzene is used as an intermediate in organic synthesis for the production of pharmaceuticals. Its unique structure allows for the creation of various drug molecules, contributing to the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-1-isopropoxy-4-nitrobenzene serves as an intermediate in the synthesis of agrochemicals. Its properties enable the production of effective compounds for crop protection and pest control.
Used in Fine Chemicals Industry:
2-Bromo-1-isopropoxy-4-nitrobenzene is also utilized as an intermediate in the synthesis of other fine chemicals. Its versatility in organic synthesis makes it valuable for the production of specialty chemicals used in various applications, such as fragrances, dyes, and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 191602-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,0 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 191602-42:
(8*1)+(7*9)+(6*1)+(5*6)+(4*0)+(3*2)+(2*4)+(1*2)=123
123 % 10 = 3
So 191602-42-3 is a valid CAS Registry Number.

191602-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-4-nitro-1-propan-2-yloxybenzene

1.2 Other means of identification

Product number -
Other names 3-Bromo-4-isopropoxynitrobenzene

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:191602-42-3 SDS

191602-42-3Relevant articles and documents

BETA-SUBSTITUTED BETA-AMINO ACIDS AND ANALOGS AS CHEMOTHERAPEUTIC AGENTS AND USES THEREOF

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Paragraph 0842, (2017/02/28)

β-Substituted β-amino acids, β-substituted β-amino acid derivatives, and β-substituted β-amino acid analogs and (bio)isosteres and their use as chemotherapeutic agents are disclosed. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and (bio)isosteres are selective LAT1/4F2hc substrates and exhibit rapid uptake and retention in tumors expressing the LAT1/4F2hc transporter. Methods of synthesizing the β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and methods of using the compounds for treating cancer are also disclosed. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs exhibit selective uptake in tumor cells expressing the LAT1/4F2hc transporter and accumulate in cancerous cells when administered to a subject in vivo. The β-substituted β-amino acid derivatives and β-substituted β-amino acid analogs and (bio)isosteres exhibit cytotoxicity toward several tumor types.

Activated pyridinium-tagged ruthenium complexes as efficient catalysts for ring-closing metathesis

Rix, Diane,Clavier, Hervé,Coutard, Yann,Gulajski, Lukasz,Grela, Karol,Mauduit, Marc

, p. 5397 - 5405 (2007/10/03)

New pyridinium-tagged ruthenium catalysts have been synthesised to perform olefin metathesis in several media including both organic and aqueous solvents and room temperature ionic liquids (RTILs). High activity was obtained in the ring-closing metathesis (RCM) of a variety of di- or tri-substituted and/or oxygen-containing dienes. However, only fair levels of recycling combined with low to moderate residual ruthenium levels (25-173 ppm) have been observed showing clearly the difficulty of associating high activity and recyclability.

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