TCI B6610, tert-butyl (4-aminobicyclo[2.1.1]hexan-1-yl)carbamate, is a mono-Boc-protected bridged diamine building block. The free primary amine allows selective acylation, urea formation, or reductive alkylation before the second nitrogen is unmasked under acidic conditions. Its rigid bicyclo[2.1.1]hexane framework fixes the distance and orientation between the two nitrogen handles. AMI Scientific offers this TCI reagent in a 100 mg pack size for medicinal chemistry and synthetic research laboratories.
—
| Brand | — |
|---|---|
| CAS number | — |
| Molecular formula | — |
| Purity | — |
| Category | — |
| Pack sizes | — |
| Physical form | — |
| Storage | — |
—
- Chmovzh et al. (2021). tert-Butyl Bis(4′-(Hexyloxy)-[1,1′-biphenyl]-4-yl)carbamate. Molbank doi:10.3390/m1247
- (2009). MILD AND EFFICIENT ONE-POT CURTIUS REARRANGEMENT: PREPARATION OF N-tert-BUTYL ADAMANTANYL-1-YL-CARBAMATE. Organic Syntheses doi:10.15227/orgsyn.086.0113
- (2022). Diasterocontrol Synthesis of Tamiflu Intermediate of Tert- butyl(5-hydroxy-6-(1-ethylpropoxy)-1,2-epoxycyclohex- 3-en-1-yl)carbamate. MALAYSIAN JOURNAL OF CHEMISTRY doi:10.55373/mjchem.v24i2.258
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
![tert-Butyl (4-Aminobicyclo[2.1.1]hexan-1-yl)carbamate (CAS 1050890-47-5) - TCI B6610 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510B6610.jpg?v=1767094023&width=1445)

