8,8-Diapocarotenedioic acid

• CAS: 27876-94-4
• Catalog Number: ACM27876944
• Category: Other Products
• Molecular Weight: 328.4
• Molecular Formula: C₂₀H₂₄O₄
• Synonyms: CROCETIN;CROCETIN, TRANS-;8,8-DIAPOCAROTENEDIOIC ACID;2,6,11,15-TETRAMETHYLHEXADECA-2,4,6,8,10,12,14-HEPTAENEDOIC ACID;TRANS-CROCETIN;8,8-diapo-psi,psi-carotenedioic acid;8,8-Diapo-ψ,ψ-carotene-8,8-dioic acid;Alpha-Crocetin

Custom Q&A

What is the molecular formula of 8,8-Diapocarotenedioic acid?

The molecular formula of 8,8-Diapocarotenedioic acid is C20H24O4.

What is the molecular weight of 8,8-Diapocarotenedioic acid?

The molecular weight of 8,8-Diapocarotenedioic acid is 328.4 g/mol.

What are some synonyms of 8,8-Diapocarotenedioic acid?

Some synonyms of 8,8-Diapocarotenedioic acid include Crocetin, Transcrocetin, trans-Crocetin, and Crocetin(2-).

What is the IUPAC name of 8,8-Diapocarotenedioic acid?

The IUPAC name of 8,8-Diapocarotenedioic acid is (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethylhexadeca-2,4,6,8,10,12,14-heptaenedioic acid.

What is the InChI of 8,8-Diapocarotenedioic acid?

The InChI of 8,8-Diapocarotenedioic acid is InChI=1S/C20H24O4/c1-15(11-7-13-17(3)19(21)22)9-5-6-10-16(2)12-8-14-18(4)20(23)24/h5-14H,1-4H3,(H,21,22)(H,23,24)/b6-5+,11-7+,12-8+,15-9+,16-10+,17-13+,18-14+.

What is the InChIKey of 8,8-Diapocarotenedioic acid?

The InChIKey of 8,8-Diapocarotenedioic acid is PANKHBYNKQNAHN-MQQNZMFNSA-N.

What is the canonical SMILES of 8,8-Diapocarotenedioic acid?

The canonical SMILES of 8,8-Diapocarotenedioic acid is CC(=CC=CC=C(C)C=CC=C(C)C(=O)O)C=CC=C(C)C(=O)O.

What is the CAS number of 8,8-Diapocarotenedioic acid?

The CAS number of 8,8-Diapocarotenedioic acid is 27876-94-4.

How many rotatable bonds are present in 8,8-Diapocarotenedioic acid?

There are 8 rotatable bonds present in 8,8-Diapocarotenedioic acid.

What is the exact mass of 8,8-Diapocarotenedioic acid?

The exact mass of 8,8-Diapocarotenedioic acid is 328.16745924 g/mol.

Synthetic Use

Upstream Synthesis Route 1

• 42553-65-1

• 27876-94-4

Reference: [1] Patent: WO2004/78695, 2004, A1, . Location in patent: Page 16

Upstream Synthesis Route 2

• 55750-86-2

• 27876-94-4

Reference: [1] Fitoterapia, 2018, vol. 129, p. 62 - 72

Upstream Synthesis Route 3

• 35482-80-5

• 27876-94-4

Reference: [1] Helvetica Chimica Acta, 1971, vol. 54, p. 2447 - 2459

Upstream Synthesis Route 4

• 35482-80-5

• 27876-94-4

Reference: [1]Helvetica Chimica Acta,1971,vol. 54,p. 2447 - 2459

Downstream Synthesis Route 1

• 27876-94-4

• 72504-47-3

Reference: [1]Helvetica Chimica Acta,1979,vol. 62,p. 1944 - 1951

Downstream Synthesis Route 2

• 27876-94-4
• 541-41-3

• 72504-48-4

Reference: [1]Helvetica Chimica Acta,1979,vol. 62,p. 1944 - 1951

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