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6574-98-7

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6574-98-7 Usage

Chemical Properties

white to almost white crystalline powder

Uses

Used as intermediate for the synthesis of agrochemicals, pharmaceuticals and chemical intermediates.

Synthesis Reference(s)

Synthetic Communications, 25, p. 2993, 1995 DOI: 10.1080/00397919508011431

Check Digit Verification of cas no

The CAS Registry Mumber 6574-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6574-98:
(6*6)+(5*5)+(4*7)+(3*4)+(2*9)+(1*8)=127
127 % 10 = 7
So 6574-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H3Cl2N/c8-6-2-1-5(4-10)7(9)3-6/h1-3H

6574-98-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A10113)  2,4-Dichlorobenzonitrile, 98%   

  • 6574-98-7

  • 5g

  • 357.0CNY

  • Detail
  • Alfa Aesar

  • (A10113)  2,4-Dichlorobenzonitrile, 98%   

  • 6574-98-7

  • 25g

  • 1427.0CNY

  • Detail
  • Alfa Aesar

  • (A10113)  2,4-Dichlorobenzonitrile, 98%   

  • 6574-98-7

  • 100g

  • 4279.0CNY

  • Detail

6574-98-7SDS

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 2,4-Dichlorobenzonitrile

1.2 Other means of identification

Product number -
Other names 4-Dichlorobenzonitrile

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:6574-98-7 SDS

6574-98-7Relevant articles and documents

Investigation of BiVO4 structure variations on the dichlorotoluene ammoxidation performance

Li, Xiongjian,Huang, Chi

, p. 866 - 870 (2020/12/30)

In this study, BiVO4 synthesized by hydrothermal and calcination methods were explored as catalysts in the ammoxidation of dichlorotoluenes to shed light on the structure-reactivity correlations. The BiVO4 samples were characterized by X-ray diffraction (XRD), temperature-programmed reduction (TPR), Brunauer–Emmett–Teller (BET), and UV–Vis spectrophotometry. The results showed that the catalytic activity of BiVO4 greatly relied on the structure variations. The hydrothermal prepared BiVO4 exhibited better catalytic activities as a consequence of its greater structure deformation, with maximum yields of 73.1, 72.2, and 70.8% for 3,4-, 2,4- and 2,6- dichlorobenzonitrles, respectively.

SO 2 F 2 -Promoted Dehydration of Aldoximes: A Rapid and Simple Access to Nitriles

Ding, Chengrong,Mei, Guangyao,Wang, Haibo,Zhang, Guofu,Zhao, Yiyong

, p. 1484 - 1488 (2019/07/15)

A rapid, simple and mild process for the dehydration of aldoximes to give the corresponding nitriles, which utilizes SO 2 F 2 as an efficient reagent, has been developed. A variety of (hetero)arene, alkene, alkyne and aliphatic aldoximes proceeded with high efficiency to afford nitriles in excellent to quantitative yields with great functional group compatibilities in acetonitrile under ambient conditions. Furthermore, an eco-friendly synthetic protocol to access nitriles from aldehydes with ortho -, meta - and para -nitrile groups was also described in aqueous methanol by using inorganic base Na 2 CO 3, and a one-pot synthetic strategy to generate nitriles from aldehydes was proved to be feasible.

Aerobic Oxidative Dehydrogenation of Amines Catalyzed by a Recoverable Ruthenium Catalyst under Mild Reaction Conditions

Karimi, Babak,Yari, Omolbanin,Khorasani, Mojtaba,Vali, Hojatollah,Mansouri, Fariborz

, p. 1783 - 1787 (2018/01/27)

A highly active catalyst based on perruthenate ions supported inside the channels of periodic mesoporous organosilica with a bridged imidazolium ionic liquid framework (Ru@PMO-IL) was developed. The material was found to be an efficient, durable, and recoverable catalyst for the oxidative dehydrogenation of various types of amines such as benzylic, aliphatic, and cyclic aliphatic amines under mild reaction conditions. The products were obtained in excellent yields with excellent selectivities.

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