2207-27-4 Usage
Description
1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is a chemical compound characterized by its yellow liquid appearance. It is known for its ability to form endo-adducts with 1,3-cyclopentadiene, which makes it a versatile compound in various applications across different industries.
Uses
Used in Chemical Synthesis:
1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is used as a key intermediate in the synthesis of various organic compounds. Its unique chemical properties allow it to form endo-adducts with 1,3-cyclopentadiene, which can be further utilized in the creation of complex molecules and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is used as a building block for the development of new drugs. Its ability to form endo-adducts can be exploited to create novel molecular structures with potential therapeutic applications.
Used in Material Science:
1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is used as a component in the development of advanced materials. Its chemical reactivity and ability to form endo-adducts make it a valuable asset in the creation of new polymers, plastics, and other materials with specific properties.
Used in Agrochemical Industry:
In the agrochemical industry, 1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is used as a starting material for the synthesis of various pesticides and other agrochemicals. Its unique chemical properties can be harnessed to develop new compounds with improved efficacy and reduced environmental impact.
Used in Dye and Pigment Industry:
1,2,3,4-Tetrachloro-5,5-dimethoxycyclopentadiene is used as a precursor in the production of dyes and pigments. Its yellow color and chemical reactivity make it a suitable candidate for the development of new colorants with enhanced properties, such as improved stability and color intensity.
Check Digit Verification of cas no
The CAS Registry Mumber 2207-27-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2207-27:
(6*2)+(5*2)+(4*0)+(3*7)+(2*2)+(1*7)=54
54 % 10 = 4
So 2207-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl4O2/c1-12-7(13-2)5(10)3(8)4(9)6(7)11/h1-2H3
2207-27-4Relevant articles and documents
Labelled compounds. XV. Hexachlorocyclopentadiene (14C) from hexachloropropene (1,3 14C) and cis 1,2 dichloroethylene
Zorkendorfer
, p. 463 - 473 (1973)
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INHIBITORS OF MTOR-DEPTOR INTERACTIONS AND METHODS OF USE THEREOF
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Page/Page column 42, (2018/05/24)
Provided herein are substituted hydrazone compounds useful as inhibitors of DEPTOR. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention also provides medical uses of substituted hydrazone compounds.
Catalytic Enantioselective Desymmetrization of Norbornenoquinones via C(sp2)-H Alkylation
Sarkar, Rahul,Mukherjee, Santanu
supporting information, p. 6160 - 6163 (2016/12/09)
The enantioselective Diels-Alder (DA) reaction with monosubstituted p-benzoquinones is an unmet challenge. A new approach for the enantioselective synthesis of monosubstituted quinone-DA adducts is presented based on C(sp2)-H alkylative desymmetrization of meso-DA adducts. Catalyzed by a tertiary amino-thiourea derivative, this reaction utilizes nitroalkanes as the alkylating agents and generates densely functionalized products bearing at least four contiguous stereogenic centers remote from the reaction site with excellent enantioselectivities.