3,4-Pyridinedicarboxylic anhydride

• CAS: 4664-08-8
• Catalog Number: ACM4664088-1
• Category: Pyridines
• Molecular Weight: 149.10
• Molecular Formula: C7H3NO3
• Synonyms: Cinchomeronic anhydride
• Canonical SMILES: O=C1OC(=O)c2cnccc12
• InChI: 1S/C7H3NO3/c9-6-4-1-2-8-3-5(4)7(10)11-6/h1-3H
• InChI Key: KFKMGUPDWTWQFM-UHFFFAOYSA-N
• Melting Point: 75-77 °C (lit.)
• Appearance: White powder
• Application: This product is suitable for scientific research.
• Assay: 97%
• Features And Benefits: 1. High quality products; 2. Fast delivery; 3. Additional products can be ordered, please contact us for details
• MDL Number: MFCD00010680
• NACRES: NA.23
• PubChem ID: 24857065
• Quality Level: 100

Custom Q&A

What is the product name of the chemical with cas number 4664-08-8?

The product name is 3,4-Pyridinedicarboxylic anhydride.

What is the molecular weight of 3,4-Pyridinedicarboxylic anhydride?

The molecular weight is 149.10.

What category does 3,4-Pyridinedicarboxylic anhydride belong to?

It belongs to CHO Containing Functional Groups.

What is the appearance of 3,4-Pyridinedicarboxylic anhydride?

It appears as white powder.

What is the assay percentage of 3,4-Pyridinedicarboxylic anhydride?

The assay percentage is 97%.

What is the melting point range of 3,4-Pyridinedicarboxylic anhydride?

The melting point range is 75-77 °C (lit.).

What are some synonyms for 3,4-Pyridinedicarboxylic anhydride?

Cinchomeronic anhydride.

What is the molecular formula of 3,4-Pyridinedicarboxylic anhydride?

The molecular formula is C7H3NO3.

What are some features and benefits of 3,4-Pyridinedicarboxylic anhydride?

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

Can additional products be ordered along with 3,4-Pyridinedicarboxylic anhydride?

Yes, additional products can be ordered.

Synthetic Use

Upstream Synthesis Route 1

• 490-11-9

• 4664-08-8

Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 22, p. 5891 - 5899

Upstream Synthesis Route 2

• 490-11-9

• 4664-08-8

Reference: [1]Gribble, Gordon W.; Saulnier, Mark G.; Obaza-Nutaitis, Judy A.; Ketcha, Daniel M.
[Journal of Organic Chemistry, 1992, vol. 57, # 22, p. 5891 - 5899]

Downstream Synthesis Route 1

• 60-35-5
• 4664-08-8

• 4664-01-1

Reference: [1] Journal of Organic Chemistry, 1949, vol. 14, p. 97,101

Downstream Synthesis Route 2

• 4664-08-8

• 4664-01-1

Reference: [1] Acta Chimica Hungarica, 1983, vol. 112, # 4, p. 487 - 500
[2] Tetrahedron Letters, 1993, vol. 34, # 39, p. 6225 - 6228
[3] Farmaco, Edizione Scientifica, 1980, vol. 35, # 11, p. 940 - 944
[4] Acta Poloniae Pharmaceutica, 1995, vol. 52, # 3, p. 245 - 248

Downstream Synthesis Route 3

• 60-35-5
• 4664-08-8

• 4664-01-1

Reference: [1]Journal of Organic Chemistry,1949,vol. 14,p. 97,101

Downstream Synthesis Route 4

• 67-56-1
• 4664-08-8

• 24202-74-2

Reference: [1]Sato, Ippei; Morihira, Koichiro; Inami, Hiroshi; Kubota, Hirokazu; Morokata, Tatsuaki; Suzuki, Keiko; Iura, Yosuke; Nitta, Aiko; Imaoka, Takayuki; Takahashi, Toshiya; Takeuchi, Makoto; Ohta, Mitsuaki; Tsukamoto, Shin-ichi
[Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 18, p. 8607 - 8618]

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