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(3aR,​3'aR,​8aS,​8'a'S)​​-2,​2'-​Cyclopropylidenebis[​3a,​8a-​dihydro-8H-​Indeno[1,​2-​d]​oxazole], 98%|9135421|229184-98-9

(3aR,3'aR,8aS,8'a'S)-2,2'-Cyclopropylidenebis[3a,8a-dihydro-8H-Indeno[1,2-d]oxazole], 98%

Cat. No JK9135421_50_MG
J&K Chemical

Product Information

Product Name
(3aR,​3'aR,​8aS,​8'a'S)​​-2,​2'-​Cyclopropylidenebis​3a,​8a-​dihydro-8H-​Indeno1,​2-​d​oxazole, 98%
Brand Name
J&K
Product Number
9135421
CAS
229184-98-9
Molecular Formula
C23H20N2O2
Molecular Weight
356.43
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11245230
IUPAC Name
(3aS,8bR)-2-1-(3aS,8bR)-4,8b-dihydro-3aH-indeno1,2-d1,3oxazol-2-ylcyclopropyl-4,8b-dihydro-3aH-indeno1,2-d1,3oxazole
InChI Key
QFXUVUBVPPOPQZ-VNTMZGSJSA-N
SMILES
C1CC1(C2=NC@H3C@@H(O2)CC4=CC=CC=C34)C5=NC@H6C@@H(O5)CC7=CC=CC=C67

Safety Information

Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Nickel-Catalyzed Enantioselective Hydromonofluoromethylation of Alkenes
Publication Name: Science of Synthesis
Publication Date: 2025

C(sp)—C(sp3) Bond Formation
Publication Name: Science of Synthesis
Publication Date: 2025

C—C Bond Formation with Hypervalent Iodine Reagents
Publication Name: Science of Synthesis
Publication Date: 2025

Functionalization by Hydrogen-Atom-Transfer C—H Activation
Publication Name: Science of Synthesis
Publication Date: 2023

Recent Advances in Transition-Metal-Catalyzed Asymmetric Functionalization of Enamides
Publication Name: Synthesis
Publication Date: 2022-08-18
DOI: 10.1055/a-1892-5473

(3aR,3'aR,8aS,8'a'S)-2,2'-Cyclopropylidenebis[3a,8a-dihydro-8H-Indeno[1,2-d]oxazole], 98%

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