132414-78-9 Usage
General Description
Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is a chemical compound with the molecular formula C19H27NO2. It is a carboxylate ester with a benzyl group attached to a six-membered ring containing nitrogen and oxygen atoms. Ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is commonly used in organic synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. It also has potential applications in the field of medicinal chemistry for the development of new drugs. Due to its complex structure and functional groups, ethyl 1-benzylhexahydropyrrolo[3,4-b]pyrrole-5(1H)-carboxylate is of interest to researchers and chemists for further study and exploration of its properties and potential uses.
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.
