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58966-27-1

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58966-27-1 Usage

General Description

1-(2-Methyl-5-nitro-phenyl)-ethanone is a chemical compound with the molecular formula C9H9NO3. It is a yellow solid that is commonly used in the synthesis of various pharmaceuticals and organic compounds. The compound has a methyl group attached to the second carbon of the phenyl ring and a nitro group attached to the fifth carbon. It is mainly used as an intermediate in the production of dyes, perfumes, and other organic compounds. The compound is also known for its mild to moderate toxicity, and proper handling and storage are required to prevent any adverse effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 58966-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,6 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58966-27:
(7*5)+(6*8)+(5*9)+(4*6)+(3*6)+(2*2)+(1*7)=181
181 % 10 = 1
So 58966-27-1 is a valid CAS Registry Number.

58966-27-1SDS

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 1-(2-methyl-5-nitrophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(2-methyl-5-nitrophenyl)ethan-1-one

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:58966-27-1 SDS

58966-27-1Relevant articles and documents

BETA-SUBSTITUTED GAMMA-AMINO ACIDS AND ANALOGS AS CHEMOTHERAPEUTIC AGENTS

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, (2015/09/22)

β-Substituted γ-amino acids, β-substituted γ-amino acid derivatives, and β-substituted γ-amino acid analogs and (bio)isosteres and their use as chemotherapeutic agents are disclosed. The β-substituted γ-amino acid derivatives and β-substituted γ-amino acid analogs and (bio)isosteres are selective LAT1/4F2hc substrates, capable of passing through the blood-brain barrier, and exhibit rapid uptake and retention in tumors expressing the LAT1/4F2hc transporter. Methods of synthesizing the β-substituted γ-amino acid derivatives and β-substituted γ-amino acid analogs and (bio)isosteres and methods of using the compounds for treating tumors are also disclosed. The β-substituted γ-amino acid derivatives and β-substituted γ-amino acid analogs and (bio)isosteres exhibit an improved selectivity toward tumor cells expressing the LAT1/4F2hc transporter and accumulate in cancerous cells when administered to a subject in vivo. The β-substituted γ-amino acid derivatives and β-substituted γ-amino acid analogs and (bio)isosteres exhibit an increased efficacy on a variety of tumor types.

2,6-Dinitroaniline herbicides

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, (2008/06/13)

The invention is substituted 2,6-dinitroaniline compounds and preemergence herbicidal methods and compositions employing the substituted 2,6-dinitroaniline compounds.

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