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1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is a chemical compound characterized by a cyclopropane ring and a carboxylic acid functional group. It is derived from 2,6-dichlorophenyl, which is a compound with two chlorine atoms attached to a phenyl ring. This unique structure and reactivity make it a promising candidate for various applications in medicinal chemistry, organic synthesis, and potentially as a precursor in the synthesis of other chemical compounds.

1039931-24-2

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1039931-24-2 Usage

Uses

Used in Medicinal Chemistry:
1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is used as a building block for the creation of more complex molecules for [application reason]. Its reactivity and structural features enable the formation of a wide range of organic compounds with diverse applications.
Used as a Precursor in Chemical Synthesis:
1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is used as a precursor in the synthesis of other chemical compounds for [application reason]. Its unique structure and reactivity make it a valuable starting material for the development of new compounds with specific properties and potential applications in various industries.
Used in Pharmaceutical Industry:
1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is used as an active pharmaceutical ingredient (API) for [application reason]. Its potential biological activity and unique structure make it a promising candidate for the development of new drugs with specific therapeutic effects.
Used in Chemical Research:
In the field of chemical research, 1-(2,6-dichlorophenyl)cyclopropane-1-carboxylic acid is used as a model compound for [application reason]. Its unique structure and reactivity provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge and understanding.

Check Digit Verification of cas no

The CAS Registry Mumber 1039931-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,9,9,3 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1039931-24:
(9*1)+(8*0)+(7*3)+(6*9)+(5*9)+(4*3)+(3*1)+(2*2)+(1*4)=152
152 % 10 = 2
So 1039931-24-2 is a valid CAS Registry Number.

1039931-24-2Downstream Products

1039931-24-2Relevant academic research and scientific papers

Synthesis of 3-oxoesters and functional derivatives of pyrimidin-4(3Н)-one based on 1-(2,6-dihalophenyl)cyclopropan-1-carboxylic acids

Novakov,Yablokov,Navrotskii,Mkrtchyan,Vernigora,Babushkin,Kachala,Ruchko

, p. 224 - 230 (2017/04/13)

Special features of the synthesis and chemical transformations of novel functional derivatives of 6-[1-(2,6-dihalophenyl)cyclopropyl]pyrimidin-4(3H)-one and ethyl esters of 3-[1-(2,6-dihalophenyl)cyclopropyl]-2-methyl-3-oxopropanoic acids prepared from 2-(2,6-dihalophenyl)acetonitriles have been revealed. Novel achiral structural analogs of experimental anti-HIV agent МС-1501 have been synthesized.

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