132414-78-9 Usage
Description
Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is a complex carboxylate ester chemical compound characterized by the molecular formula C19H27NO2. It features a benzyl group attached to a six-membered ring that includes nitrogen and oxygen atoms, making it a versatile intermediate in organic synthesis and a promising candidate for pharmaceutical and agrochemical development.
Uses
Used in Pharmaceutical Industry:
Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and functional groups contribute to the development of new drugs, particularly in medicinal chemistry where its properties are being further explored for potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate serves as an essential component in the creation of novel agrochemicals. Its role as an intermediate allows for the production of compounds that can address specific agricultural needs, such as pest control and crop protection.
Used in Organic Synthesis:
Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is utilized as a versatile building block in organic synthesis. Its complex structure and the presence of multiple functional groups make it a valuable precursor for the synthesis of a wide range of organic compounds, including those with potential applications in various industries.
Used in Research and Development:
Due to its intriguing structure and potential applications, Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is a subject of interest for researchers and chemists. It is used in the exploration of new properties and potential uses, driving innovation and advancement in the fields of chemistry and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 132414-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,1 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132414-78:
(8*1)+(7*3)+(6*2)+(5*4)+(4*1)+(3*4)+(2*7)+(1*8)=99
99 % 10 = 9
So 132414-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H22N2O2/c1-2-20-16(19)18-11-14-8-9-17(15(14)12-18)10-13-6-4-3-5-7-13/h3-7,14-15H,2,8-12H2,1H3
132414-78-9Relevant articles and documents
DOPAMINE D3 RECEPTOR ANTAGONISTS HAVING A BICYCLO MOIETY
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Paragraph 0631; 0632, (2017/02/28)
The disclosure provides compounds having formula (I), wherein the substituents are as defined herein. The compounds are useful for modulating the dopamine D3 receptor and for treating conditions associated therewith, such as addictions, drug dependency, and psychiatric conditions.
Preparation of 2,7-diazabicyclo[3.3.0]octanes
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, (2008/06/13)
2,7-Diazabicyclo[3.3.0]octanes, suitable for 7-position substituents or antibacterially active quinolone carboxylic acids, of the formula STR1 in which R1, R3, R4, R5, R7 and R8 may be identical or different and in each case denote H, C1 -C5 -alkyl (optionally substituted by halogen, hydroxyl or C1 -C3 -alkoxy), C1 -C3 -alkoxycarbonyl or C6 -C12 -aryl, R4 additionally denotes halogen, R2 and R6 may be identical or different, denote H, C1 -C6 -alkyl, benzyl, C6 -C12 -aryl, C1 -C3 -alkanoyl, benzoyl or C1 -C5 -alkoxycarbonyl, or R2 and R3 together denote a bridge of the structure (CH2)n, n=2-4, CH2 --CHOH--CH2, CH2 --S--CH2 or C(CH3)2 --S--CH2, excluding 2,7-diazabicyclo[3.3.0]octane. Also their preparation by the reaction STR2 Intermediates II are also new.
