tert-Butyl rac-(4aS,7aS)-hexahydropyrrolo[3,4-b][1,4]oxazine-4(4aH)-carboxylate

tert-Butyl rac-(4aS,7aS)-hexahydropyrrolo[3,4-b][1,4]oxazine-4(4aH)-carboxylate

(3aR,6aS)-Octahydro-3a,6a-dimethyl-2-(phenylmethyl)pyrrolo[3,4-c]pyrrole

(3aR,6aS)-Octahydro-3a,6a-dimethyl-2-(phenylmethyl)pyrrolo[3,4-c]pyrrole

trans-tert-butyl hexahydropyrrolo[3,4-b][1,4]oxazine-6(2H)-carboxylate

$300.00
CAS No.: 138026-93-4
Catalog No.: 192573
Purity: 95%
MF: C11H20N2O3
MW: 228.292
Storage: 2-8 degree Celsius
SMILES: O1[C@H]2[C@H](NCC1)CN(C2)C(=O)OC(C)(C)C
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192573
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trans-tert-butyl hexahydropyrrolo[3,4-b][1,4]oxazine-6(2H)-carboxylate; CAS No.: 138026-93-4; trans-tert-butyl hexahydropyrrolo[3,4-b][1,4]oxazine-6(2H)-carboxylate. PROPERTIES: Trans-tert-butyl hexahydropyrrolo[3,4-b][1,4]oxazine-6(2H)-carboxylate presents as a pale yellow crystalline powder with a characteristic ester odor. The compound demonstrates moderate polarity with a logP approximately 2.5 and shows good solubility in polar aprotic solvents. It exhibits typical ester hydrolysis kinetics under basic conditions. Recommended storage involves maintaining in tightly sealed containers away from moisture. Safety data indicates potential for skin irritation necessitating protective clothing during handling as per GHS classification P337+P313. APPLICATIONS: Trans-tert-butyl hexahydropyrrolo[3,4-b][1,4]oxazine-6(2H)-carboxylate serves as an intermediate in the preparation of muscle relaxants documented in neuromuscular pharmacology research. Its hexahydropyrrolooxazine framework enables asymmetric synthesis applications in pharmaceutical development as reported in stereochemistry journals. Furthermore, the compound contributes to synthesis of fluorescent probes for protein detection described in bioanalytical chemistry innovations.

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