76064-23-8 Usage
Description
Sodium 3-cyanoprop-1-enoxide is a chemical compound with the molecular formula C3H3NNaO. It is a derivative of propenoic acid, containing a cyanide group at the third carbon position and a sodium ion. Sodium 3-cyanoprop-1-enoxide is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds. It is also utilized in the production of pharmaceuticals, agrochemicals, and dyes. When handled and used properly, sodium 3-cyanoprop-1-enoxide can be an important tool in chemical research and manufacturing processes.
Uses
Used in Organic Synthesis:
Sodium 3-cyanoprop-1-enoxide is used as a reagent for the formation of carbon-carbon bonds in organic synthesis. Its unique structure allows for the creation of new chemical linkages, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, sodium 3-cyanoprop-1-enoxide is used as a key intermediate in the synthesis of various drugs. Its ability to form carbon-carbon bonds makes it a valuable component in the development of new medicinal compounds.
Used in Agrochemical Production:
Sodium 3-cyanoprop-1-enoxide is also utilized in the production of agrochemicals, such as pesticides and herbicides. Its role in creating carbon-carbon bonds is essential for the synthesis of these compounds, which are used to protect crops and enhance agricultural productivity.
Used in Dye Production:
In the dye industry, sodium 3-cyanoprop-1-enoxide is used as a starting material for the synthesis of various dyes. Its ability to form carbon-carbon bonds contributes to the creation of a wide range of colored compounds used in textiles, printing, and other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 76064-23-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,6 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76064-23:
(7*7)+(6*6)+(5*0)+(4*6)+(3*4)+(2*2)+(1*3)=128
128 % 10 = 8
So 76064-23-8 is a valid CAS Registry Number.
76064-23-8Relevant articles and documents
3 - Ethoxy acrylonitrile and 3, 3 - diethyl dimethoxypropionitrile is treated mixture of synthetic method
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Paragraph 0037; 0038; 0039; 0040-0048, (2019/07/05)
The invention belongs to the field of medicinal chemistry, in particular to medicinal chemistry of the in the field of organic synthesis, more in particular to 3 - ethoxy acrylonitrile and 3, 3 - diethyl dimethoxypropionitrile is treated mixture of synthetic method. The method uses acetonitrile with a ester alcohol under the action of the alkali metal salt, to obtain the intermediate compound II, then this compound II and then under the action of the phase transfer catalyst, with the sulfuric acid b b obtained by the target mixture compound I, namely 3 - ethoxy acrylonitrile and 3, 3 - diethyl dimethoxypropionitrile is treated mixture. The invention disclosed 3 - ethoxy acrylonitrile and 3, 3 - diethyl dimethoxypropionitrile is treated mixture of the synthetic method has low material cost, relatively mild reaction conditions, the operation is simple, the yield and the like, which is suitable for the industrial production, application of the method.
Synthesis and reactivity of pyrrolo[3,2-d][1,3]oxazine-2,4-dione. Access to new pyrrolo[3,2-e][1,4]diazepine-2,5-diones
Malcor, Jean-Daniel,Brouillette, Yann,Graffion, Julien,Spielmann, Kim,Masurier, Nicolas,Maillard, Ludovic T.,Martinez, Jean,Lisowski, Vincent
, p. 4631 - 4639 (2014/06/23)
A convenient synthesis of pyrrolo[3,2-d][1,3]oxazine-2,4-dione 4 is described and its reactivity towards various nucleophiles studied. The regioselective ring opening of anhydride 4 or its N-alkylated analog 25 in the presence of alanine or proline afforded, respectively, imidazolidinedione 22 and N-protected pyrrolo[3,2-e][1,4]diazepines 30 and 31 in a one-pot process. In a last part of this study, an alternative route to produce a library of eight non protected pyrrolo[3,2-e][1,4]diazepine-2,5-diones 35a-h is described to overcome the limited reactivity of anhydride 4.