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Chemical structure of CAS 21850-12-4

Octahydroisoindole

In Stock•Starting at $12 for 5 g•Purity ≥ 97%
CAS No.21850-12-4
MDL No.MFCD03265253
MFC8H15N
MW125.21
InChI KeyODSNARDHJFFSRH-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
5 g97%$12In Stock
10 g97%$17In Stock
25 g97%$38In Stock
100 g97%$140In Stock
500 g97%$689In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

CAS No.21850-12-4
Product NameOctahydroisoindole
IrritantIrritant
Signal Word:Warning
HCode:H302-H315-H319-H335
PCode:P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Benzyl 2-benzyl-4-[(3aS,7aR)-2,3,3a,4,5,6,7,7a-octa-hydro-1H-isoindol-2-yl]-4-oxobutano-ate.

Acta crystallographica. Section E, Structure reports online • Vol. 68, Issue Pt 10 • 2012
PMID: 23125656PMC: PMC3470212DOI: 10.1107/S1600536812037567

Synthesis and pharmacological characterization of bicyclic triple reuptake inhibitor 3-aryl octahydrocyclopenta[c]pyrrole analogues.

Journal of medicinal chemistry • Vol. 54, Issue 15 • 2011
PMID: 21739935DOI: 10.1021/jm101312a

Total synthesis of (±)-kainic acid: a photochemical C-H carbamoylation approach.

Organic letters • Vol. 13, Issue 10 • 2011
PMID: 21504139DOI: 10.1021/ol200772f

Remodelling of the natural product fumagillol employing a reaction discovery approach.

Nature chemistry • Vol. 3, Issue 12 • 2011
PMID: 22213919PMC: PMC3254213DOI: 10.1038/nchem.1178

Documentation

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