CAS 121412-39-3

1,2-Naphthalenediol, 4-(cyclohexylmethylamino)-, 1,2-diacetate

Description:

1,2-Naphthalenediol, 4-(cyclohexylmethylamino)-, 1,2-diacetate, identified by its CAS number 121412-39-3, is a chemical compound that features a naphthalene backbone substituted with hydroxyl groups and an amino group. This compound is characterized by its diacetate functional groups, which enhance its solubility and reactivity. The presence of the cyclohexylmethylamino moiety suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the structural diversity it introduces. The hydroxyl groups contribute to its potential as a hydrogen bond donor, influencing its interactions in biological systems. Additionally, the compound may exhibit interesting optical properties due to the naphthalene structure, which can be relevant in various applications, including organic electronics and dyes. Overall, the unique combination of functional groups in this compound suggests a range of potential applications, particularly in the fields of organic synthesis and drug development.

Formula: C₂₁H₂₅NO₄

InChI: InChI=1S/C21H25NO4/c1-14(23)25-20-13-19(22(3)16-9-5-4-6-10-16)17-11-7-8-12-18(17)21(20)26-15(2)24/h7-8,11-13,16H,4-6,9-10H2,1-3H3

InChI key: InChIKey=DABSYCZQZRNORX-UHFFFAOYSA-N

SMILES: O(C(C)=O)C=1C2=C(C(N(C)C3CCCCC3)=CC1OC(C)=O)C=CC=C2

Synonyms:

• CGS 21595
• 1,2-Naphthalenediol, 4-(cyclohexylmethylamino)-, diacetate (ester)
• 1,2-Naphthalenediol, 4-(cyclohexylmethylamino)-, 1,2-diacetate

CGS 21595

CAS: 121412-39-3

CGS 21595 inhibits the formation of 5-hydroxyeicosatetraenoic acid and leukotriene B4; rapidly metabolized to CGS 19213.

Formula: C₂₁H₂₅NO₄

Color and Shape: Solid

Molecular weight: 355.43

Ref: TM-T71221