Welcome to LookChem.com Sign In|Join Free

CAS

  • or
4,5-DICHLORO-2-NITROTOLUENE is an organic compound with the molecular formula C7H5Cl2NO2. It is characterized by the presence of two chlorine atoms at the 4th and 5th positions, and a nitro group (-NO2) at the 2nd position on a toluene ring. 4,5-DICHLORO-2-NITROTOLUENE is typically used as a reagent in various chemical syntheses and has potential applications in the pharmaceutical and biotechnology industries.

7494-45-3

Post Buying Request

7494-45-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7494-45-3 Usage

Uses

Used in Pharmaceutical Industry:
4,5-DICHLORO-2-NITROTOLUENE is used as a reagent for the synthesis of N-hydroxyindole-2-carboxylates, which are inhibitors of lactate dehydrogenase (LDH). These inhibitors play a crucial role in controlling cancer cell proliferation, making 4,5-DICHLORO-2-NITROTOLUENE a valuable asset in the development of anticancer drugs.
Used in Biotechnology Industry:
In the biotechnology sector, 4,5-DICHLORO-2-NITROTOLUENE is utilized in the preparation of polyhalogenated quinoline C-nucleosides. These compounds have the potential to serve as antiviral agents, contributing to the development of new treatments for viral infections.
Used in Research:
4,5-DICHLORO-2-NITROTOLUENE is also suitable for LDH-related research, providing a foundation for further exploration into the mechanisms of lactate dehydrogenase and its role in various diseases, including cancer. By understanding the interactions between 4,5-DICHLORO-2-NITROTOLUENE and LDH, researchers can gain insights into the development of more effective therapies for cancer and other LDH-related conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7494-45-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7494-45:
(6*7)+(5*4)+(4*9)+(3*4)+(2*4)+(1*5)=123
123 % 10 = 3
So 7494-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Cl2NO2/c1-4-2-5(8)6(9)3-7(4)10(11)12/h2-3H,1H3

7494-45-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Dichloro-2-Nitrotoluene

1.2 Other means of identification

Product number -
Other names 1,2-dichloro-4-methyl-5-nitrobenzene

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:7494-45-3 SDS

7494-45-3Relevant articles and documents

Preparation method of dichlorotoluene nitride intermediate

-

Sheet 0035-0039; 0054; 0065, (2021/01/28)

The invention belongs to the technical field of preparation of pesticide intermediates, and particularly discloses a preparation method of a dichlorotoluene nitride intermediate. The preparation method comprises the following steps: fully reacting raw materials, a solvent and a nitration reagent to obtain a dichlorotoluene nitride intermediate, wherein the raw materials comprise any one of o-dichlorotoluene, m-dichlorotoluene and p-dichlorotoluene; the solvent is dichloroethane; the nitration reagent is concentrated nitric acid; the dichlorotoluene nitride intermediate is shown as a chemical formula 7 and a chemical formula 12. The preparation method has the advantages that the corrosion to reaction equipment is less, and the generation and discharge of waste acid and waste salt in the production process are greatly reduced.

METHODS USING HDAC11 INHIBITORS

-

Paragraph 0639-0640, (2018/05/16)

The present invention provides methods and uses of inhibitors of histone deacetylase 11 (HDAC11) in the treatment of diseases and/or disorders, such as, for example, cell proliferative diseases.

Synthesis and structure-activity relationships of a series of substituted 2-(1H-furo[2,3-g]indazol-1-yl)ethylamine derivatives as 5-HT2C receptor agonists

Shimada, Itsuro,Maeno, Kyoichi,Kazuta, Ken-ichi,Kubota, Hideki,Kimizuka, Tetsuya,Kimura, Yasuharu,Hatanaka, Ken-ichi,Naitou, Yuki,Wanibuchi, Fumikazu,Sakamoto, Shuichi,Tsukamoto, Shin-ichi

, p. 1966 - 1982 (2008/09/21)

A series of novel indazole derivatives were synthesized, and their structure-activity relationships examined in order to identify potent and selective 5-HT2C receptor agonists. Among these compounds, (S)-2-(7-ethyl-1H-furo[2,3-g]indazol-1-yl)-1-methylethylamine (YM348) had a good in vitro profile, that is, high agonistic activity to the human 5-HT2C receptor subtype (EC50 = 1.0 nM) and high selectivity over 5-HT2A receptors. This compound was also effective in a rat penile erection model when administered po.

BENZENESULFONAMIDE INHIBITOR OF CCR2 CHEMOKINE RECEPTOR

-

Page/Page column 33-34, (2010/11/25)

Disclosed are compounds of formula (I): or a pharmaceutically acceptable salt thereof, or a solvate thereof, or a combination thereof, as well as compositions of methods of use of the compound, wherein R1, R2, R3, and m ar

CYCLIC AMIDINES USEFUL AS NMDA NR2B ANTAGONISTS

-

, (2008/06/13)

The invention encompasses novel compounds of Formula I as well as a method of treating NMDA mediated diseases comprising administration to a patient in need of such treatment a non-toxic amount of a compound of Formula I effective to block the NMDA NR2B r

Bis(dealkoxycarbonylation) of nitroarylmalonates: A facile entry to alkylated nitroaromatics

Gurjar,Reddy,Murugaiah,Murugaiah

, p. 1659 - 1661 (2007/10/03)

A simple approach to alkylated nitroaromatics from substituted nitroaryl malonic esters by double decarboxylation is detailed.

5-(5,6-Dichloro-2-indolyl)-2-methoxy-2,4-pentadienamides: Novel and selective inhibitors of the vacuolar H+-ATPase of osteoclasts with bone antiresorptive activity

Gagliardi, Stefania,Nadler, Guy,Consolandi, Emanuela,Parini, Carlo,Morvan, Marcel,Legave, Marie-N?elle,Belfiore, Pietro,Zocchetti, Andrea,Clarke, Geoffrey D.,James, Ian,Nambi, Ponnal,Gowen, Maxine,Farina, Carlo

, p. 1568 - 1573 (2007/10/03)

The vacuolar H+-ATPase (V-ATPase), located on the ruffled border of the osteoclast, is a proton pump which is responsible for secreting the massive amounts of protons that are required for the bone resorption process. With the aim to identify n

Transition metal catalysed cross-coupling between benzylic halides and aryl nucleophiles. Synthesis of some toxicologically interesting tetrachlorobenzyltoluenes

De Lang, Robbert-Jan,Van Hooijdonk, Marcel J.C.M.,Brandsma, Lambert,Kramer, Hester,Seinen, Willem

, p. 2953 - 2966 (2007/10/03)

The aryl-benzyl cross-coupling in the presence of copper-, nickel- and palladium-catalysts has been investigated with a number of chlorine- and methyl-substituted arylmetal compounds ArM (M = MgBr, ZnCl) and (substituted) benzylic halides ArCH2X. The results have been applied in the selective synthesis of some toxicologically interesting tetrachlorobenzyltoluenes.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7494-45-3