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83820-75-1

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83820-75-1 Usage

Compound type

Chemical compound

Class

Organic compounds, pyrrolizine carboxylic acids

Presence

Found in trace amounts in certain plants

Uses

Research and experimental applications, pharmaceutical development, starting material for synthesis of other organic compounds

Safety

Handle with caution and in accordance with proper safety protocols due to potential reactivity and hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 83820-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,8,2 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83820-75:
(7*8)+(6*3)+(5*8)+(4*2)+(3*0)+(2*7)+(1*5)=141
141 % 10 = 1
So 83820-75-1 is a valid CAS Registry Number.

83820-75-1Downstream Products

83820-75-1Relevant articles and documents

Synthesis of ethyl 1,2-dihydro-3H-pyrrolopyrrole-1-carboxylate by an intramolecular carbenoid reaction

Galeazzi, Edvige,Guzman, Angel,Pinedo, Araceli,Saldana, Adolfo,Torre, Diana,Muchowski, Joseph M.

, p. 454 - 456 (2007/10/02)

Cupric ion (or copper) or boron trifluoride promoted decomposition of ethyl 2-diazo-4-(pyrrol-1-yl)butanonate 6 produced mixtures of the title compound 7 and cis and trans ethyl 4-(pyrrol-1-yl)buten-2-oates 9 and 10.The formation of 7 by these processes represents the first reported instances of the intramolecular attack of an α-oxocarbenoid or a Lewis acid complexed α-diazoalkylcarboalkoxy function on the pyrrole nucleus.

5-(2-Pyrroyl)-1,2-dihydro-3H-pyrrolo?1,2-a!pyrrole-1-carboxylic acid derivatives and process for the production thereof

-

, (2008/06/13)

Novel 5-(2-pyrroyl) and 5-(N-lower alkyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo?1,2-a!pyrrole-1-carboxylic acid compounds represented by the formula: STR1 and the pharmaceutically acceptable, non-toxic esters and salts thereof, wherein each of R and R1 is independently hydrogen or a lower alkyl group having from 1 to 4 carbon atoms and process for the production of such compounds; 5-(N-methyl-2-pyrroyl)-1,2-dihydro-3H-pyrrolo?1,2-a!pyrrole-1-carboxylic acid is representative of the class. These compounds are useful as anti-inflammatory analgesic and anti-pyretic agents and as smooth muscle relaxants.

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