3,6-Dichlorophthalic anhydride

• CAS: 4466-59-5
• Catalog Number: ACM4466595-1
• Category: Polymer/Macromolecule
• Molecular Weight: 217.01
• Molecular Formula: C₈H₂Cl₂O₃
• Synonyms: 4,7-Dichloroisobenzofuran-1,3-dione
• Canonical SMILES: Clc1ccc(Cl)c2C(=O)OC(=O)c12
• InChI: 1S/C8H2Cl2O3/c9-3-1-2-4(10)6-5(3)7(11)13-8(6)12/h1-2H
• InChI Key: HEGLMCPFDADCAQ-UHFFFAOYSA-N
• Melting Point: 188-190 °C (lit.)
• Application: This product is suitable for scientific research.
• Assay: 98%
• EC Number: 224-733-2
• Features And Benefits: 1. High quality products; 2. Fast delivery; 3. Additional products can be ordered, please contact us for details
• MDL Number: MFCD00042786
• PubChem ID: 24862113
• Quality Level: 200

Custom Q&A

What is the product name of the chemical with CAS number 4466-59-5?

The product name is 3,6-Dichlorophthalic anhydride.

What is the category of 3,6-Dichlorophthalic anhydride?

It belongs to the category of Halogen Functional Groups.

What is the molecular weight of 3,6-Dichlorophthalic anhydride?

The molecular weight is 217.01.

What is the molecular formula of 3,6-Dichlorophthalic anhydride?

The molecular formula is C8H2Cl2O3.

What is the melting point of 3,6-Dichlorophthalic anhydride?

The melting point is 188-190 °C (lit.).

What is the assay percentage of 3,6-Dichlorophthalic anhydride?

The assay percentage is 98%.

What are some features and benefits of 3,6-Dichlorophthalic anhydride?

Some features and benefits include high-quality products, fast delivery, and the option to order additional products.

What is the EC Number of 3,6-Dichlorophthalic anhydride?

The EC Number is 224-733-2.

What is the Beilstein REAXYS Number of 3,6-Dichlorophthalic anhydride?

The Beilstein REAXYS Number is 164697.

Can 3,6-Dichlorophthalic anhydride be used for scientific research?

Yes, this product is suitable for scientific research.

Synthetic Use

Upstream Synthesis Route 1

• 16110-99-9

• 4466-59-5

Reference: [1] Justus Liebigs Annalen der Chemie, 1887, vol. 238, p. 357

Upstream Synthesis Route 2

• 117-21-5

• 4466-59-5
• 88389-98-4

Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 20, p. 5532 - 5535

Upstream Synthesis Route 3

• 62268-16-0

• 4466-59-5

Reference: [1] Journal of Heterocyclic Chemistry, 1995, vol. 32, # 3, p. 907 - 914
[2] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 19, p. 2755 - 2758

Upstream Synthesis Route 4

• 117-21-5

• 4466-59-5
• 88389-98-4

Reference: [1]Journal of Organic Chemistry,1992,vol. 57,p. 5532 - 5535