10467-10-4 Usage
Uses
Used in Organic Synthesis:
Ethylmagnesium iodide is used as a nucleophilic reagent for the formation of carbon-carbon bonds, which is crucial in the synthesis of a wide range of organic compounds. Its ability to donate the ethyl group makes it a versatile component in the creation of alcohols, ketones, and esters.
Used in Grignard Reactions:
In the field of organic chemistry, ethylmagnesium iodide is employed as a key component in Grignard reactions. These reactions involve the coupling of the ethyl group with various electrophiles, leading to the formation of new carbon-carbon bonds and the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
Ethylmagnesium iodide is used as a synthetic intermediate in the production of certain pharmaceuticals. Its role in forming carbon-carbon bonds is essential in the synthesis of drug molecules, contributing to the development of new medications.
Used in Material Science:
Ethylmagnesium iodide is utilized in the synthesis of advanced materials, such as polymers and composites, where the formation of carbon-carbon bonds is necessary for creating the desired material properties. Its reactivity allows for the creation of novel materials with unique characteristics.
Used in Research and Development:
In academic and industrial research settings, ethylmagnesium iodide is used as a tool for exploring new reaction pathways and developing innovative synthetic methods. Its reactivity and versatility make it a valuable asset in the pursuit of new discoveries in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 10467-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,6 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10467-10:
(7*1)+(6*0)+(5*4)+(4*6)+(3*7)+(2*1)+(1*0)=74
74 % 10 = 4
So 10467-10-4 is a valid CAS Registry Number.
10467-10-4Relevant articles and documents
Substituted isoindolones useful as plant growth regulators
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, (2008/06/13)
Substituted isoindolones I STR1 where R1 and R2 =H, unsubstituted or substituted alkyl, alkenyl, alkynyl, cyano, C1 -C6 -alkoxycarbonyl, formyl, C1 -C6 -alkylcarbonyl, unsubstituted or subs
Piperazinobutyrophenone derivatives
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, (2008/06/13)
Central nervous system active butyrophenone derivatives in which γ -piperazinobutyrophenone derivatives of the formula, SPC1 Wherein R1 is hydrogen, amino, C1 -C5 alkanoylamino, C1 -C4 alkylamino or N-(C1 -C4 alkyl)(C1 -C5 alkanoyl) amino; R2 is hydrogen or halogen; R3 is hydrogen, halogen, C1 -C4 alkyl, C1 -C4 alkoxy or trifluoromethyl; and m is 0, 1 or 2, and acid addition salts thereof, can be prepared by reacting an indole derivative of the formula, SPC2 Wherein R2, R3 and m are the same as defined above, and R4 and R5 are hydrogen or C1 -C4 alkyl respectively, with an oxidizing agent to yield an o-alkanoylamino-γ-piperazinobutyrophenone derivative of the formula, SPC3 Wherein R2, R3, R4, R5 and m are the same as defined above, and further, if necessary, hydrolyzing the product to yield an o-amino-γ-piperazinobutyrophenone derivative of the formula, SPC4 Wherein R2, R3, R5 and m are the same as defined above, and further diazotizing, if desired, in case R5 is hydrogen, the obtained o-amino-γ-piperazinobutyrophenone derivative and subsequently decomposing the resultant diazonium compound to replace the diazonium group by hydrogen. Among the butyrophenone derivatives thus obtained, those in which R1 is amino, alkanoylamino, alkylamino or N-alkylalkanoylamino and those in which R1 is hydrogen and R2 is halogen substituted at meta-position to carbonyl group are novel compounds.
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