51318-98-0 Usage
General Description
2-(carboxymethyl)bicyclo[2.2.1]hept-5-ene-2-carboxylic acid is a chemical compound with a bicyclic structure containing a carboxymethyl group and two carboxylic acid functional groups. It is a derivative of bicyclo[2.2.1]hept-5-ene, a bicyclic hydrocarbon. 2-(carboxymethyl)bicyclo[2.2.1]hept-5-ene-2-carboxylic acid has potential applications in pharmaceuticals, as the bicyclic structure can impart unique properties to drug molecules. Additionally, it can be used in organic synthesis and as a building block in the production of specialty chemicals. It also has the potential to be used in the development of new materials and polymers due to its unique structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 51318-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,1 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51318-98:
(7*5)+(6*1)+(5*3)+(4*1)+(3*8)+(2*9)+(1*8)=110
110 % 10 = 0
So 51318-98-0 is a valid CAS Registry Number.
51318-98-0Relevant articles and documents
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Tate,Bavley
, p. 6519 (1957)
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A direct route to angularly substituted hydrindanes. Formal synthesis of bakkenolide-A and synthesis of an advanced intermediate to umbellactal
Maity, Soumitra,Ghosh, Subrata
scheme or table, p. 9202 - 9210 (2010/01/16)
A direct route for the synthesis of highly functionalized angularly substituted hydrindanes has been developed. The key step involves RO-RCM of an appropriately functionalized norbornene derivative. The hydrindane derivative obtained in this way has been
Strategic use of retro Diels-Alder reaction in the construction of β-carboxy-α-methylene-γ-lactones. Total synthesis of methylenolactocin and protolichesterinic acid
Ghatak, Anjan,Sarkar, Subrata,Ghosh, Subrata
, p. 17335 - 17342 (2007/10/03)
A facile route for the construction of β-carboxy-α-methylene-γ-lactone unit is described using retro Diels-Alder reaction as the key step. Using this protocol, total synthesis of (±)-methylenolactocin and (±)-protolichesterinic acid has been achieved.
