1-(6-Nitro-1,3-benzodioxol-5-yl)ethanol

• CAS: 159873-64-0
• Catalog Number: ACM159873640
• Category: Photolabile Protection Reagents
• Molecular Weight: 211.17
• Molecular Formula: C9H9NO5
• Synonyms: α-Methyl-6-nitro-1,3-benzodioxole-5-methanol; α-Methyl-6-nitropiperonyl Alcohol
• IUPAC Name: 1-(6-nitro-1,3-benzodioxol-5-yl)ethanol
• Canonical SMILES: CC(C1=CC2=C(C=C1[N+](=O)[O-])OCO2)O
• InChI Key: UHJMDARCOIYCHL-UHFFFAOYSA-N
• Exact Mass: 211.04800
• Physical State: Solid

Synthetic Use

Upstream Synthesis Route 1

• 56136-84-6

• 159873-64-0

Reference: [1] Journal of the American Chemical Society, 1997, vol. 119, # 22, p. 5081 - 5090
[2] Helvetica Chimica Acta, 2001, vol. 84, # 12, p. 3735 - 3741
[3] Organic Letters, 2007, vol. 9, # 14, p. 2649 - 2651

Upstream Synthesis Route 2

• 712-97-0

• 159873-64-0

Reference: [1] Organic and Biomolecular Chemistry, 2017, vol. 15, # 24, p. 5117 - 5120

Upstream Synthesis Route 3

• 3162-29-6

• 159873-64-0

Reference: [1] Helvetica Chimica Acta, 2001, vol. 84, # 12, p. 3735 - 3741
[2] Journal of the American Chemical Society, 1997, vol. 119, # 22, p. 5081 - 5090

Downstream Synthesis Route 1

• 7693-46-1
• 159873-64-0

• 865872-19-1

Reference: [1]Journal of the American Chemical Society,1995,vol. 117,p. 12050 - 12057
[2]Bioorganic and Medicinal Chemistry Letters,2005,vol. 15,p. 3917 - 3920

Downstream Synthesis Route 2

• 530-62-1
• 159873-64-0
• 50-89-5

• 156876-22-1

Reference: [1]Journal of Organic Chemistry,1995,vol. 60,p. 6270 - 6276

Downstream Synthesis Route 3

• 75-44-5
• 159873-64-0

• 156876-26-5

Reference: [1]Journal of the American Chemical Society,2004,vol. 126,p. 4088 - 4089
[2]Journal of the American Chemical Society,1997,vol. 119,p. 5081 - 5090

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