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2',5'-Dichloroacetophenone is an organic compound characterized by its clear yellow to brownish liquid appearance. It is known for its chemical properties and is utilized in various applications across different industries.

2476-37-1

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2476-37-1 Usage

Uses

Used in Chemical Synthesis:
2',5'-Dichloroacetophenone is used as a chemical intermediate for the synthesis of various organic compounds. Its role in the synthesis of 5-chloro-2-(2-thienylthio)acetophenone exemplifies its utility in creating complex molecules for further applications.
Used in Research and Development:
In the field of chemistry, 2',5'-dichloroacetophenone is employed as a subject of study for understanding the standard molar enthalpy of formation in the condensed phase. This research contributes to the broader knowledge of chemical properties and reactions involving 2',5'-Dichloroacetophenone.
While the provided materials do not explicitly mention other industries or specific applications, it is worth noting that 2',5'-dichloroacetophenone, like many organic compounds, may have potential uses in various sectors such as pharmaceuticals, materials science, or as a reagent in laboratory settings. Its specific applications would depend on the requirements and innovations within those fields.

Check Digit Verification of cas no

The CAS Registry Mumber 2476-37-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2476-37:
(6*2)+(5*4)+(4*7)+(3*6)+(2*3)+(1*7)=91
91 % 10 = 1
So 2476-37-1 is a valid CAS Registry Number.

2476-37-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A13770)  2',5'-Dichloroacetophenone, 98%   

  • 2476-37-1

  • 5g

  • 358.0CNY

  • Detail
  • Alfa Aesar

  • (A13770)  2',5'-Dichloroacetophenone, 98%   

  • 2476-37-1

  • 10g

  • 614.0CNY

  • Detail
  • Alfa Aesar

  • (A13770)  2',5'-Dichloroacetophenone, 98%   

  • 2476-37-1

  • 25g

  • 1058.0CNY

  • Detail
  • Alfa Aesar

  • (A13770)  2',5'-Dichloroacetophenone, 98%   

  • 2476-37-1

  • 100g

  • 3936.0CNY

  • Detail

2476-37-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,5-dichlorophenyl)ethanone

1.2 Other means of identification

Product number -
Other names 2,5-Dichloroacetophenone

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:2476-37-1 SDS

2476-37-1Relevant articles and documents

Irsogladine maleate preparation method

-

Paragraph 0009; 0010, (2019/05/16)

The invention belongs to the field of organic matter synthesis, and particularly relates to an irsogladine maleate preparation method, wherein p-dichlorobenzene is used as a starting raw material, andfive reactions of acetylation, bromoform reaction, cyanation, cyclization and salt formation are performed to prepare the target compound. According to the present invention, the new irsogladine maleate preparation method is used, can significantly accelerate the reaction rate and improve the yield, has advantages of cost reducing, environment protection, simple operation and convenient post-treatment, and is suitable for industrial production.

Transformation of Alkynes into Chiral Alcohols via TfOH-Catalyzed Hydration and Ru-Catalyzed Tandem Asymmetric Hydrogenation

Liu, Sensheng,Liu, Huan,Zhou, Haifeng,Liu, Qixing,Lv, Jinliang

supporting information, p. 1110 - 1113 (2018/02/23)

A novel full atom-economic process for the transformation of alkynes into chiral alcohols by TfOH-catalyzed hydration coupled with Ru-catalyzed tandem asymmetric hydrogenation in TFE under simple conditions has been developed. A range of chiral alcohols was obtained with broad functional group tolerance, good yields, and excellent stereoselectivities.

One-pot synthesis of chiral alcohols from alkynes by CF3SO3H/ruthenium tandem catalysis

Liu, Huan,Liu, Sensheng,Zhou, Haifeng,Liu, Qixing,Wang, Chunqin

, p. 14829 - 14832 (2018/04/30)

A practical one-pot synthesis of chiral alcohols from readily available alkynes via tandem catalysis by the combination of CF3SO3H and a fluorinated chiral diamine Ru(ii) complex in aqueous CF3CH2OH is described. Very interestingly, the combination of fluorinated catalysts and solvent exhibits a positive fluorine effect on the reactivity and enantioselectivity. A range of chiral alcohols with wide functional group tolerance was obtained in high yield and excellent stereoselectivity under simple and mild conditions.

ANTI-HCMV COMPOSITIONS AND METHODS

-

Page/Page column 95; 96, (2016/06/06)

This document relates to compounds useful as agents for preventing or treating human cytomegalovirus (HCMV) infections.

Microwave-assisted dehalogenation of α-haloketones by zinc and ammonium chloride in alcohol

Li, Jian,Ye, Deju,Liu, Hong,Luo, Xiaoming,Jiang, Hualiang

, p. 567 - 575 (2008/04/12)

The treatment of α-haloketones with 1.5 equiv. of Zn and 1 equiv. of NH4Cl in ethanol for 0.5αmin gave the corresponding ketones with excellent yields under microwave irradiation. Vic-dibromides and 2,2-dibromoacetophenone can be efficiently debrominated to alkenes and acetophenones, respectively. Copyright Taylor & Francis Group, LLC.

Process for the preparation of halogenated hydroxydiphenyl compounds

-

, (2008/06/13)

There is described a process for the preparation of halogenated hydroxydiphenyl compounds of formula (1) by acylation of a halogenated benzene compound (first stage), etherification of the acylated compound with a halogenated phenol compound, which is not further substituted in the ortho-position (second stage), oxidation of the etherified compound (third stage) and hydrolysis of the oxidized compound in a fourth stage, wherein the reaction of the second stage is carried out in the presence of K2CO3 and any desired copper catalyst, where K2CO3 is used in a concentration of from 0.5 to 30 mol, based on the phenol compound employed of formula (6), according to the reaction scheme (I) in which R1 and R2 independently of one another are F, Cl or Br; R3 and R4 independently of one another are hydrogen; or C1-C4alkyl; m is 1 to 3; and n is 1 or 2. The compounds of formula (1) are used for protecting organic materials and articles from microorganisms.

Process for the preparation of halogenated hydroxydiphenyl compounds

-

, (2008/06/13)

A process for the preparation of halohydroxydiphenyl compounds useful for protecting organic materials and articles from microorganisms, of the formula by acylation of a halogenated benzene compound (first stage), etherification of the acylated compound with a halogenated phenol compound (second stage), oxidation of the etherified compound (third stage) and hydrolysis of the oxidized compound in a fourth stage, according to the following reaction scheme: in which R1 and R2 independently of one another are F, Cl or Br; R3 and R4 independently of one another are hydrogen; or C1-C4alkyl; m is 1 to 3; and n is 1 or 2.

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