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99-54-7

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99-54-7 Usage

Chemical Properties

colourless to yellow crystals or beige powder

Uses

Different sources of media describe the Uses of 99-54-7 differently. You can refer to the following data:
1. 1,2-Dichloro-4-nitrobenzene is an intermediate in the synthesis of agrochemicals. Studies have been conducted to use 1,2-Dichloro-4-nitrobenzene as an organic intermediate for the synthetic preparati on of ciprofloxacin (C482500).
2. 1,2-Dichloro-4-nitrobenzene is an intermediate in the synthesis of agrochemicals. Studies have been conducted to use 1,2-Dichloro-4-nitrobenzene as an organic intermediate for the synthetic preparation of ciprofloxacin (C482500).

Synthesis Reference(s)

The Journal of Organic Chemistry, 42, p. 3494, 1977 DOI: 10.1021/jo00442a009

General Description

Colorless crystals or light beige solid.

Air & Water Reactions

Insoluble in water.

Fire Hazard

3,4-Dichloronitrobenzene is combustible.

Flammability and Explosibility

Nonflammable

Purification Methods

Crystallise it from absolute EtOH. [Beilstein 5 IV 726.]

Check Digit Verification of cas no

The CAS Registry Mumber 99-54-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99-54:
(4*9)+(3*9)+(2*5)+(1*4)=77
77 % 10 = 7
So 99-54-7 is a valid CAS Registry Number.

99-54-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (A10620)  1,2-Dichloro-4-nitrobenzene, 99%   

  • 99-54-7

  • 250g

  • 279.0CNY

  • Detail
  • Alfa Aesar

  • (A10620)  1,2-Dichloro-4-nitrobenzene, 99%   

  • 99-54-7

  • 1000g

  • 897.0CNY

  • Detail
  • Alfa Aesar

  • (A10620)  1,2-Dichloro-4-nitrobenzene, 99%   

  • 99-54-7

  • 5000g

  • 1334.0CNY

  • Detail
  • Sigma-Aldrich

  • (35831)  1,2-Dichloro-4-nitrobenzene  PESTANAL®, analytical standard

  • 99-54-7

  • 35831-1G

  • 313.56CNY

  • Detail
  • Aldrich

  • (D68800)  1,2-Dichloro-4-nitrobenzene  99%

  • 99-54-7

  • D68800-100G

  • 341.64CNY

  • Detail

99-54-7SDS

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 1,2-Dichloro-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1,2-dichloro-4-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:99-54-7 SDS

99-54-7Relevant articles and documents

Doyle et al.

, p. 3494 (1977)

Nitration of deactivated aromatic compounds via mechanochemical reaction

Wu, Jian-Wei,Zhang, Pu,Guo, Zhi-Xin

supporting information, (2021/05/05)

A variety of deactivated arenes were nitrated to their corresponding nitro derivatives in excellent yields under high-speed ball milling condition using Fe(NO3)3·9H2O/P2O5 as nitrating reagent. A radical involved mechanism was proposed for this facial, eco-friendly, safe, and effective nitration reaction.

Completely-continuous flow synthesis method of 3,4-dichloronitrobenzene under action of catalyst

-

Paragraph 0070-0082, (2020/05/30)

The invention discloses a completely-continuous flow synthesis method of 3,4-dichlonitrobenzene under the action of a catalyst. The completely-continuous flow synthesis method is carried out in an integrated completely-continuous flow reaction system, a reaction substrate and other raw materials are uninterruptedly added at a feed port, the product 3, 4-dichloronitrobenzene is uninterruptedly obtained at a discharge port, and the synthesis method is safe and efficient and has no amplification effect. Compared with a traditional production method, the method of the invention has the advantagesof shortening of the production time to be within 120 seconds, no amplification effect, stable product index and good reproducibility.

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