7,8-Dihydroxy-6-methoxycoumarin

• CAS: 574-84-5
• Catalog Number: ACM574845-2
• Category: Polymer/Macromolecule
• Molecular Weight: 208.17
• Molecular Formula: C₁₀H₈O₅
• Synonyms: Fraxetin
• Canonical SMILES: COc1cc2C=CC(=O)Oc2c(O)c1O
• InChI: 1S/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3
• InChI Key: HAVWRBANWNTOJX-UHFFFAOYSA-N
• Melting Point: 230-231 °C (lit.)
• Application: This product is suitable for scientific research.
• Assay: 98%
• EC Number: 209-376-2
• Features And Benefits: 1. High quality products; 2. Fast delivery; 3. Additional products can be ordered, please contact us for details
• MDL Number: MFCD00006873
• NACRES: NA.23
• Packaging: Packaging; 250 mg in glass bottle
• PubChem ID: 24855272
• Quality Level: 100

Custom Q&A

What is the product name of the compound with CAS number 574-84-5?

The product name is 7,8-Dihydroxy-6-methoxycoumarin.

What is the molecular weight of 7,8-Dihydroxy-6-methoxycoumarin?

The molecular weight is 208.17.

What is the molecular formula of 7,8-Dihydroxy-6-methoxycoumarin?

The molecular formula is C10H8O5.

Can additional products related to 7,8-Dihydroxy-6-methoxycoumarin be ordered?

Yes, additional products can be ordered. Contact the supplier for details.

What is the melting point of 7,8-Dihydroxy-6-methoxycoumarin?

The melting point is 230-231 °C.

What is the assay percentage of 7,8-Dihydroxy-6-methoxycoumarin?

The assay percentage is 98%.

What is the application of 7,8-Dihydroxy-6-methoxycoumarin?

The product is suitable for scientific research.

What are the features and benefits of 7,8-Dihydroxy-6-methoxycoumarin?

High quality products, fast delivery, and additional products can be ordered.

How is 7,8-Dihydroxy-6-methoxycoumarin packaged?

It is packaged in a 250 mg glass bottle.

What is the PubChemID of 7,8-Dihydroxy-6-methoxycoumarin?

The PubChemID is 24855272.

Synthetic Use

Downstream Synthesis Route 1

• 908094-01-9
• 574-84-5

• 486-21-5
• 525-21-3

Reference: [1]Spaeth; Jerzmanowska-Sienkiewiczowa
[Chemische Berichte, 1937, vol. 70, p. 1672,1676]

Downstream Synthesis Route 2

• 574-84-5
• 108-24-7

• 73815-12-0

Reference: [1]McCullagh et al.
[Transactions of the Royal Society of Canada, 1929, vol. <3> 23V, p. 159,162]
[2]Kondo et al.
[Nippon Nogeikagaku Kaishi, 1955, vol. 29, p. 950][Chem.Abstr., 1958, p. 21 076]
[3]Shimada
[Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1952, vol. 72, p. 67][Chem.Abstr., 1952, p. 6328]
Shimada
[Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1937, vol. 57, p. 618,621; dtsch. Ref. S. 148, 150][Chem.Abstr., 1939, p. 2653]
[4]Parthasarathy, M. R.; Pardha Saradhi, K.
[Phytochemistry, 1984, vol. 23, # 4, p. 867 - 870]

Downstream Synthesis Route 3

• 574-84-5
• 77-78-1

• 6035-49-0

Reference: [1]Son, Dong Ju; Lee, Gyung Rak; Oh, Sungil; Lee, Sung Eun; Choi, Won Sik
[Nutrients, 2015, vol. 7, # 3, p. 1945 - 1964]
[2]Kondo et al.
[Nippon Nogeikagaku Kaishi, 1955, vol. 29, p. 950][Chem.Abstr., 1958, p. 21 076]

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