(S)-3-Amino-gamma-butyrolactone hydrochloride

• CAS: 117752-82-6
• Catalog Number: ACM117752826
• Category: Other Products
• Molecular Weight: 137.56
• Molecular Formula: C₄H₇NO₂.ClH
• Synonyms: (S)-3-Amino-gamma-butyrolactone hydrochloride, 117752-82-6, PubChem14757, SureCN6776803, KSC498C4F, CTK3J8142, ACT04380, ANW-46119, FD1172, SBB069904, AKOS006306175, AKOS015849556, AG-C-28434, (4S)-4-AMINOOXOLAN-2-ONE HCL, AK-41710, KB-05333, X3132
• IUPAC Name: (4S)-4-aminooxolan-2-one;hydrochloride
• Canonical SMILES: C1C(COC1=O)N.Cl
• InChI Key: MZYONVUDAOYDKV-DFWYDOINSA-N
• Exact Mass: 137.02400
• H-Bond Acceptor: 3
• H-Bond Donor: 2

Synthetic Use

Upstream Synthesis Route 1

• 79069-16-2

• 117752-82-6

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 3, p. 562 - 566
[2] Synlett, 2002, # 7, p. 1105 - 1106

Upstream Synthesis Route 2

• 91240-51-6

• 117752-82-6

Reference: [1] Patent: WO2015/63001, 2015, A1, . Location in patent: Page/Page column 19; 20

Upstream Synthesis Route 3

• 754228-95-0

• 117752-82-6

Reference: [1] Canadian Journal of Chemistry, 1988, vol. 66, p. 779 - 782

Upstream Synthesis Route 4

• 754228-95-0

• 117752-82-6

Reference: [1]Canadian Journal of Chemistry,1988,vol. 66,p. 779 - 782

Downstream Synthesis Route 1

• 1013-88-3
• 117752-82-6

• 117752-83-7

Reference: [1]Bioorganic and Medicinal Chemistry Letters,2017,vol. 27,p. 562 - 566
[2]Canadian Journal of Chemistry,1988,vol. 66,p. 779 - 782

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