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Boc-3-Hydroxy-1-adamantyl-D-glycine

group of stereoisomers with the chemical formula C₁₇H₂₇NO₅
ChemicalSubstance group_of_stereoisomers Q72449526
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Summary

Boc-3-Hydroxy-1-adamantyl-D-glycine is a group of stereoisomers[1].

Key Facts

  • Boc-3-Hydroxy-1-adamantyl-D-glycine's instance of is recorded as group of stereoisomers[2].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's CAS Registry Number is recorded as 361442-00-4[3].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's EC number is recorded as 700-361-0[4].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's canonical SMILES is recorded as CC(C)(C)OC(=O)NC(C(=O)O)C12CC3CC(CC(O)(C3)C1)C2[5].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's InChI is recorded as InChI=1S/C17H27NO5/c1-15(2,3)23-14(21)18-12(13(19)20)16-5-10-4-11(6-16)8-17(22,7-10)9-16/h10-12,22H,4-9H2,1-3H3,(H,18,21)(H,19,20)/t10-,11+,12-,16?,17?/m1/s1[6].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's InChIKey is recorded as UKCKDSNFBFHSHC-BSVBHRQSSA-N[7].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's chemical formula is recorded as C₁₇H₂₇NO₅[8].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's subclass of is recorded as chemical compound[9].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's PubChem CID is recorded as 11267340[10].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's catalog is recorded as CAS COVID-19 Anti-Viral Candidate Compounds[11].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's isomeric SMILES is recorded as CC(C)(C)OC(=O)NC@HC12C[C@H]3CC@@HCC(C3)(C2)OC@HC12C[C@H]3CC@@HCC(C3)(C2)O">[12].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+325.18892296399997'}[13].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's ECHA Substance Infocard ID is recorded as 100.148.876[14].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's SureChEMBL ID is recorded as 27218038[15].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's DSSTox substance ID is recorded as DTXSID60957561[16].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's DSSTOX compound identifier is recorded as DTXCID701385496[17].
  • Boc-3-Hydroxy-1-adamantyl-D-glycine's UniChem compound ID is recorded as 64314146[18].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Boc-3-Hydroxy-1-adamantyl-D-glycine. Retrieved May 3, 2026, from https://4ort.xyz/entity/boc-3-hydroxy-1-adamantyl-d-glycine
MLA “Boc-3-Hydroxy-1-adamantyl-D-glycine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/boc-3-hydroxy-1-adamantyl-d-glycine.
BibTeX @misc{4ortxyz_boc-3-hydroxy-1-adamantyl-d-glycine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Boc-3-Hydroxy-1-adamantyl-D-glycine}}, year = {2026}, url = {https://4ort.xyz/entity/boc-3-hydroxy-1-adamantyl-d-glycine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Boc-3-Hydroxy-1-adamantyl-D-glycine — https://4ort.xyz/entity/boc-3-hydroxy-1-adamantyl-d-glycine (retrieved 2026-05-03)

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