2,6-Dimethoxyphenol

• CAS: 91-10-1
• Catalog Number: ACM91101
• Category: Phenols
• Molecular Weight: 154.16
• Molecular Formula: C₈H₁₀O₃
• Synonyms: 6-CYCLOHEXYL-4-METHYL PYRONE;MCP;1,3-Dimethoxy-2-hydroxybenzene;1,3-Dimethyl pyrogallate;1,3-dimethylpyrogallate;2,6-dimethoxy-pheno;2,6-Dimethoxyphenol (syringol);2,6-Dimethoxyphenyl
• Boiling Point: 261°C(lit.)
• Melting Point: 50-57°C(lit.)
• Flash Point: >230°F
• Hazard Statements: Xn,Xi
• RIDADR: UN 2430 8 / PGIII
• Safety Description: 26-36-37/39
• Supplemental Hazard Statements: H301-H302-H315-H319-H335
• Symbol: GHS07,GHS06

Custom Q&A

What is the molecular formula of 2,6-Dimethoxyphenol?

The molecular formula of 2,6-Dimethoxyphenol is C8H10O3.

What are some synonyms for 2,6-Dimethoxyphenol?

Some synonyms for 2,6-Dimethoxyphenol include Syringol, Pyrogallol 1,3-dimethyl ether, and Phenol, 2,6-dimethoxy.

What is the molecular weight of 2,6-Dimethoxyphenol?

The molecular weight of 2,6-Dimethoxyphenol is 154.16 g/mol.

What are the computed descriptors for 2,6-Dimethoxyphenol?

The computed descriptors for 2,6-Dimethoxyphenol include InChI, InChIKey, and Canonical SMILES.

Where can 2,6-Dimethoxyphenol be found naturally?

2,6-Dimethoxyphenol is a natural product found in Bistorta manshuriensis, Mucuna birdwoodiana, and other organisms.

What is the exact mass of 2,6-Dimethoxyphenol?

The exact mass of 2,6-Dimethoxyphenol is 154.062994177 g/mol.

How many hydrogen bond donor counts does 2,6-Dimethoxyphenol have?

2,6-Dimethoxyphenol has 1 hydrogen bond donor count.

What is the XLogP3 value of 2,6-Dimethoxyphenol?

The XLogP3 value of 2,6-Dimethoxyphenol is 1.1.

What is the topological polar surface area of 2,6-Dimethoxyphenol?

The topological polar surface area of 2,6-Dimethoxyphenol is 38.7 Ų.

What is the Formal Charge of 2,6-Dimethoxyphenol?

The Formal Charge of 2,6-Dimethoxyphenol is not specified in the provided reference.

Synthetic Use

Upstream Synthesis Route 1

• 225793-15-7

• 824-42-0
• 91-10-1
• 148-53-8
• 95-48-7

Reference: [1] Journal of Organic Chemistry, 2000, vol. 65, # 5, p. 1376 - 1389

Upstream Synthesis Route 2

• 634-36-6

• 91-10-1

Reference: [1]Omura, Kanji
[Synthesis, 1998, # 8, p. 1145 - 1148]

Upstream Synthesis Route 3

• 530-57-4

• 91-10-1

Reference: [1]Carvalho, Christopher F.; Russo, Albert V.; Sargent, Melvyn V.
[Australian Journal of Chemistry, 1985, vol. 38, # 5, p. 777 - 792]

Downstream Synthesis Route 1

• 91-10-1

• 934-00-9
• 24677-78-9
• 148-53-8
• 95-48-7

Reference: [1] Journal of Organic Chemistry, 2000, vol. 65, # 5, p. 1376 - 1389

Downstream Synthesis Route 2

• 91-10-1

• 487-11-6

Reference: [1] Journal of the Chinese Chemical Society, 2004, vol. 51, # 5 A, p. 969 - 974
[2] Journal of Chemical Research - Part S, 2003, # 6, p. 358 - 359
[3] Justus Liebigs Annalen der Chemie, 1918, vol. 414, p. 251

Downstream Synthesis Route 3

• 91-10-1
• 6638-05-7

• 603-25-8

Reference: [1]Chemische Berichte,1878,vol. 11,p. 1459

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