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1,2,4-[1]Propanyl[3]ylidenepentalene-9-carboxylicacid,9-amino-1,2,3,3a,4,6a-hexahydro-, is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

339308-57-5

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339308-57-5 Usage

Chemical class

Amino acid derivative
1,2,4-[1]Propanyl[3]ylidenepentalene-9-carboxylicacid,9-amino-1,2,3,3a,4,6a-hexahydro-, is derived from an amino acid, which are the building blocks of proteins.

Pentalene structure

Aromatic hydrocarbon
Pentalene is a type of aromatic hydrocarbon with five carbon atoms in a ring.

Carboxylic acid group

Functional group
The carboxylic acid group (-COOH) is a functional group that can form hydrogen bonds and participate in various chemical reactions.

Propanyl group

Alkyl group
The propanyl group (C3H7) is an alkyl group derived from propane, which can be attached to other molecules to form more complex structures.

Ylidene group

Electron-rich group
The ylidenepentalene group is an electron-rich group that can participate in various chemical reactions, such as electrophilic addition.

Hexahydro derivative

Six hydrogen atoms
The term "hexahydro" indicates that the compound has six hydrogen atoms, which can affect its chemical properties and reactivity.

Pharmaceutical or biological significance

Potential applications
Due to its amino acid and carboxylic acid components, 1,2,4-[1]Propanyl[3]ylidenepentalene-9-carboxylicacid,9-amino-1,2,3,3a,4,6a-hexahydro-, may have potential applications in medicinal chemistry or drug development.

Molecular complexity

Long and complex name
The compound's name reflects its complex structure, which may have implications for its synthesis, stability, and reactivity.

Chemical reactivity

Potential for various reactions
The presence of multiple functional groups (amino, carboxylic acid, and ylidenepentalene) suggests that 1,2,4-[1]Propanyl[3]ylidenepentalene-9-carboxylicacid,9-amino-1,2,3,3a,4,6a-hexahydro-, can participate in a range of chemical reactions, such as substitution, elimination, and addition reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 339308-57-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,3,0 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 339308-57:
(8*3)+(7*3)+(6*9)+(5*3)+(4*0)+(3*8)+(2*5)+(1*7)=155
155 % 10 = 5
So 339308-57-5 is a valid CAS Registry Number.

339308-57-5Downstream Products

339308-57-5Relevant academic research and scientific papers

Enantioselective synthesis of amino acids from pentacyclo[5.4.0.02,6.03,10.05,9] undecane-8,11-dione

Martins, Frans J.C,Viljoen, Agatha M,Kruger, Hendrik G,Fourie, Louis,Roscher, Justus,Joubert, André J,Wessels, Philippus L

, p. 1601 - 1607 (2007/10/03)

Treatment of (+)-pentacyclo[5.4.0.02,6.03,10.05,9] undecane-8-one with sodium cyanide and ammonium carbonate produced an optically active hydantoin of which the 4′-carbonyl group of the hydantoin ring is in the less sterically hindered equatorial position. Hydrolysis of the latter with barium hydroxide produced (-)-8-amino-pentacyclo [5.4.0.02,6.03,10.05,9]undecane-8-carboxylic acid which has the 1S,2R,3R,5R,6R,7S,8R,9R,10R configuration. In a similar way, (+)-6-amino-tetracyclo-[6.2.0.04,11.05,9] undec-2-ene-6-carboxylic acid with 1R,4R,5R,6R,8S,9S,11R configuration was obtained from (-)-tetracyclo[6.3.0.04,11.05,9]undec-2-ene-6-one. The latter was obtained from (-)-11-hydroxy-pentacyclo [5.4.0.02,6.03,10.05,9]undecan-8-one.

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