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(+/-)-1-benzyl-(3aR,6aS)-octahydro-cyclopenta[b]pyrrole is a complex organic compound with a unique molecular structure. It consists of a cyclopenta[b]pyrrole ring system, which is a five-membered ring with a pyrrole (a nitrogen-containing ring) fused to it. The compound features an octahydro (eight hydrogen atoms) substituent, indicating the presence of a saturated hydrocarbon chain. Additionally, it has a benzyl group attached to the 1-position, which is a phenylmethyl group, providing a phenyl ring connected to a methyl group. The stereochemistry at the 3a and 6a positions is specified as R and S, respectively, indicating the specific arrangement of atoms in three-dimensional space. (+/-)-1-benzyl-(3ar,6ac)-octahydro-cyclopenta[b]pyrrole is of interest in organic chemistry and may have potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules.

2030-31-1

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2030-31-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2030-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,3 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2030-31:
(6*2)+(5*0)+(4*3)+(3*0)+(2*3)+(1*1)=31
31 % 10 = 1
So 2030-31-1 is a valid CAS Registry Number.

2030-31-1Downstream Products

2030-31-1Relevant academic research and scientific papers

Catalytic intermolecular hydroaminations of unactivated olefins with secondary alkyl amines

Musacchio, Andrew J.,Lainhart, Brendan C.,Zhang, Xin,Naguib, Saeed G.,Sherwood, Trevor C.,Knowles, Robert R.

, p. 727 - 730 (2017)

The intermolecular hydroamination of unactivated alkenes with simple dialkyl amines remains an unsolved problem in organic synthesis. We report a catalytic protocol for efficient additions of cyclic and acyclic secondary alkyl amines to a wide range of alkyl olefins with complete anti-Markovnikov regioselectivity. In this process, carbon-nitrogen bond formation proceeds through a key aminium radical cation intermediate that is generated via electron transfer between an excited-state iridium photocatalyst and an amine substrate. These reactions are redox-neutral and completely atom-economical, exhibit broad functional group tolerance, and occur readily at room temperature under visible light irradiation. Certain tertiary amine products generated through this method are formally endergonic relative to their constituent olefin and amine starting materials and thus are not accessible via direct coupling with conventional ground-state catalysts.

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