(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid|926276-11-1,AngeneChemical

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid

Request for Quotation

Chemical Name:	(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid
CAS Number:	926276-11-1
Product Number:	AG00H130(AGN-PC-0WA1PO)
Synonyms:
MDL No:
Molecular Formula:	C8H13NO2
Molecular Weight:	155.19432

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
Customer Feedback

Identification/Properties

Safety Information

GHS Pictogram:

N/A

Signal Word:

UN#:

N/A

Hazard Statements:

Precautionary Statements:

Class:

N/A

Packing Group:

N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Quantity Required:*

Company Name:

Contact Person:*

Email:*

Tel:*

Country:*

Others:(Optional)

Verification Code:

Customer Feedback

Chemical Structure

(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and reactivity make it an essential building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals.$name$ plays a crucial role in the synthesis of heterocyclic compounds, particularly in the formation of cyclic structures with pharmacological importance. Due to its specific stereochemistry and functional groups, $name$ can participate in diverse reactions such as ring-closure reactions, cycloadditions, and functional group transformations.Chemists frequently employ $name$ as a chiral auxiliary or a key intermediate to introduce chirality into complex molecules. Its utility in asymmetric synthesis enables the creation of enantiomerically pure compounds, which is essential in drug development and other areas requiring stereochemically defined molecules.Additionally, $name$ serves as a precursor in the preparation of novel materials and bioactive compounds. Its versatility in chemical transformations makes it a valuable tool for synthetic chemists seeking to access structurally diverse compounds with potential applications in various fields.Overall, the strategic incorporation of $name$ in chemical synthesis allows for the efficient construction of intricate molecular architectures and the exploration of new chemical space for the development of innovative compounds.