(1R,2R)-trans-N-Boc-2-aminocyclohexanol

• CAS: 155975-19-2
• Catalog Number: ACM155975192
• Category: Other Products
• Molecular Weight: 215.29
• Molecular Formula: C₁₁H₂₁NO₃
• Synonyms: 121282-70-0, tert-Butyl (trans-2-hydroxycyclohexyl)carbamate, tert-butyl (1R,2R)-2-hydroxycyclohexylcarbamate, PubChem19549, SureCN1670964, CTK8B7140, ANW-56486, SBB062689, ZINC34257055, AKOS015911497, RL00919, RL00920, AK101084, KB-60746, (1R,2R)-trans-N-Boc-2-aminocyclohexanol, tert-butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate, I14-36905, 155975-19-2
• IUPAC Name: tert-butyl N-[(1R,2R)-2-hydroxycyclohexyl]carbamate
• Canonical SMILES: CC(C)(C)OC(=O)NC1CCCCC1O
• InChI Key: XVROWZPERFUOCE-RKDXNWHRSA-N
• Exact Mass: 215.15200
• H-Bond Acceptor: 3
• H-Bond Donor: 2

Synthetic Use

Upstream Synthesis Route 1

• 364385-55-7

• 155975-19-2

Reference: [1] Patent: US2007/287695, 2007, A1, . Location in patent: Page/Page column 14; 55

Upstream Synthesis Route 2

• 24424-99-5
• 110716-78-4

• 155975-19-2

Reference: [1] Journal of Organic Chemistry, 2004, vol. 69, # 6, p. 1858 - 1865

Upstream Synthesis Route 3

• 24424-99-5
• 931-15-7

• 155975-19-2

Reference: [1] Journal of Organic Chemistry, 2006, vol. 71, # 6, p. 2320 - 2331
[2] Journal of the American Chemical Society, 2013, vol. 135, # 12, p. 4884 - 4892
[3] Patent: US2014/309225, 2014, A1, . Location in patent: Paragraph 1432; 1433

Downstream Synthesis Route 1

• 155975-19-2

• 931-15-7

Reference: [1]Bulletin of the Chemical Society of Japan,1994,vol. 67,p. 1196 - 1197

* For details of the synthesis route, please refer to the original source to ensure accuracy.