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2-Chloro-3-nitroaniline, a chemical compound with the molecular formula C6H5ClN2O2, is a pale yellow solid derivative of aniline. It features a nitro group and a chloro group on the aromatic ring, making it a versatile intermediate in the synthesis of various organic compounds, especially dyes and pigments.

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  • 3970-41-0 Structure
  • Basic information

    1. Product Name: 2-CHLORO-3-NITROANILINE
    2. Synonyms: Aniline, 2-chloro-3-nitro-
    3. CAS NO:3970-41-0
    4. Molecular Formula: C6H5ClN2O2
    5. Molecular Weight: 172.57
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3970-41-0.mol
  • Chemical Properties

    1. Melting Point: 95-96 °C
    2. Boiling Point: 318.2±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.494±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. PKA: 0.51±0.10(Predicted)
    10. CAS DataBase Reference: 2-CHLORO-3-NITROANILINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-CHLORO-3-NITROANILINE(3970-41-0)
    12. EPA Substance Registry System: 2-CHLORO-3-NITROANILINE(3970-41-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 3970-41-0(Hazardous Substances Data)

3970-41-0 Usage

Uses

Used in Textile Industry:
2-Chloro-3-nitroaniline is used as an intermediate in the production of dyes and pigments for textiles, providing a wide range of colors and enhancing the durability and vibrancy of fabrics.
Used in Plastics Industry:
In the plastics industry, 2-CHLORO-3-NITROANILINE is utilized as a precursor for the synthesis of colorants, contributing to the aesthetic appeal and customization of plastic products.
Used in Chemical Synthesis:
2-Chloro-3-nitroaniline serves as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals, due to its reactive functional groups.
Safety Precautions:
It is crucial to handle 2-CHLORO-3-NITROANILINE with care, as it can be harmful if ingested, inhaled, or absorbed through the skin. Proper safety measures, including the use of personal protective equipment and adherence to handling protocols, should be implemented to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 3970-41-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3970-41:
(6*3)+(5*9)+(4*7)+(3*0)+(2*4)+(1*1)=100
100 % 10 = 0
So 3970-41-0 is a valid CAS Registry Number.

3970-41-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-3-NITROANILINE

1.2 Other means of identification

Product number -
Other names chloronitroaniline

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:3970-41-0 SDS

3970-41-0Relevant articles and documents

Synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles

Huang, Shenlin,Connolly, Peter J.

, p. 9373 - 9375 (2004)

A highly efficient synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles has been developed. The key step involves intramolecular cyclization of a thiourea facilitated by the nitro group. A highly efficient synthesis of 2-N-alkyl(aryl)amino-7-nitrobenzothiazoles has been developed. The key step involves intramolecular cyclization of a thiourea facilitated by the nitro group.

Design, synthesis and herbicidal activity study of aryl 2,6-disubstituted sulfonylureas as potent acetohydroxyacid synthase inhibitors

Wei, Wei,Zhou, Shaa,Cheng, Dandan,Li, Yuxin,Liu, Jingbo,Xie, Yongtao,Li, Yonghong,Li, Zhengming

supporting information, p. 3365 - 3369 (2017/07/07)

A series of sulfonylurea derivatives containing a 2,6-disubstituted aryl moiety were designed, synthesized and evaluated for their herbicidal activities. Most of these compounds showed excellent inhibitory rates against both monocotyledonous and dicotyledonous weeds, especially 10a, 10h and 10i. They exhibited equivalent or superior herbicidal efficiency than commercial chlorsulfuron at the dosage of 15?g/ha and the preliminary SAR was summarized. In order to illuminate the molecular mechanism of several potent compounds, their apparent inhibition constant (Kiapp) of Arabidopsis thaliana acetohydroxyacid synthase (AHAS) were determined and the results confirmed that these compounds were all potent AHAS inhibitors. 10i have a Kiapp of 11.5?nM, which is about 4 times as potent as chlorsulfuron (52.4?nM).

Gold supported on titania for specific monohydrogenation of dinitroaromatics in the liquid phase

Liu, Shuang-Shuang,Liu, Xiang,Yu, Lei,Liu, Yong-Mei,He, He-Yong,Cao, Yong

, p. 4162 - 4169 (2014/09/29)

Liquid-phase selective monohydrogenation of various substituted dinitroaromatics to the corresponding valuable nitroanilines was investigated on gold-based catalysts. Special attention was paid to the effect of Au particle size on this monoreduction reaction. Interestingly, TiO2 supported gold catalysts containing a relatively larger mean Au particle size (>5 nm) showed far superior chemoselectivity for specific mono-hydrogenation of dinitroaromatics, with the highest performance attainable for the catalyst bearing Au particles of ca. 7.5 nm. Results in the intermolecular competitive hydrogenation showed that the intrinsic higher accumulation rates of the desired nitroanilines associated with the catalyst possessing larger Au particles were responsible for the high chemoselectivity observed. the Partner Organisations 2014.

Convenient chlorination of some special aromatic compounds using N-chlorosuccinimide

Gan, Zongjie,Hu, Bin,Song, Qiao,Xu, Yungen

experimental part, p. 1074 - 1078 (2012/05/04)

Some chlorinated aromatic compounds, including indole, benzofuran, carbazole, pyridine and aniline derivatives, are difficult to obtain through convenient chlorination. We herein report their efficient synthesis through chlorination with N-chlorosuccinimide (NCS). Optimization of the reaction conditions, including the temperature and the choice of solvent, was also investigated. This approach, which is characterized by a facile procedure, comparatively high yields and environmentally friendly features, provides a straightforward and inexpensive route to several chlorinated aromatic compounds. Georg Thieme Verlag Stuttgart · New York.

Heteromeric double helix formation by cross-hybridization of chloro-and fluoro-substituted quinoline oligoamides

Gan, Quan,Li, Fei,Li, Guoping,Kauffmann, Brice,Xiang, Junfeng,Huc, Ivani,Jiang, Hua

supporting information; experimental part, p. 297 - 299 (2010/05/01)

Oligoamides of 8-chloroquinoline have been synthesized and shown to assemble into double helical dimers both in solution and in the solid state, and to undergo cross-hybridization with 8-fluoroquinoline oligoamide analogues; the handedness of these double

FUSED PYRIMIDINE DERIVATIVE AND USES THEREOF

-

Page/Page column 71, (2008/06/13)

A compound represented by the formula (I) wherein ring A is a 5-membered aromatic heterocycle optionally having substituent(s), R1 is a hydrogen atom or a hydrocarbon group optionally having substituent(s), W is an oxygen atom or a sulfur atom, X1 and X2 may be the same or different and each is a hydrogen atom, a hydrocarbon group optionally having substituent(s) or a heterocyclic group, or, X1 and X2 in combination optionally form an oxygen atom, a sulfur atom or =NR2, ring B is an aromatic ring optionally further having substituent(s), Y is a bond, C1-6 alkylene C2-6 alkenylene or C2-6 alkynylene, optionally having substituent(s), and Z is a group represented by formula: -SOnR3, or a group represented by formula: -COR4, or a salt thereof, is useful as a pharmaceutical agent having GnRH antagonistic action.

Substituted N-phenyl 2-hydroxy-2-methyl-3,3,3-trifluoropropanamide derivatives which elevate pyruvate dehydrogenase activity

-

Page column 48, (2010/02/05)

A compound of formula (I) wherein: n is 1 or 2; R 1 is chloro, fluoro, bromo, methyl or methoxy; R 2 is as defined within; R 3 is as defined within; and R 4 is hydrogen or fluoro; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof is described. The use of compounds of formula (I) in the production of an elevation of PDH activity in a warm-blooded animal such as a human being are also described. Pharmaceutical compositions, methods and processes for preparation of compounds of formula (I) are detailed. STR1

Preparation and NMR analysis of 2,6-heterodifunctional halobenzenes as precursors for substituted biphenyls

Sienkowska, Monika,Benin, Vladimir,Kaszynski, Piotr

, p. 165 - 173 (2007/10/03)

Preparation and complete characterization of 16 2,6-disubstituted halobenzenes, including nine new compounds, from two common starting materials is described. Seven of the new compounds contain one or two propylthio groups, which have been introduced in two ways. Direct reaction of arenediazonium salts with 1-propanethiolate gives yields comparable to those obtained in a three-step method through sulfonyl chlorides. The 1H- and 13C NMR chemical shifts of 17 1,2,3-trisubstituted benzenes have been correlated with the predicted values and the observed trends explained using commonly available modeling packages.

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