24181-64-4

Basic information

• Product Name: Ochrobirine
• Synonyms: (5R,6'S,8'S)-6',7,8,8'-Tetrahydro-6-methylspiro[1,3-dioxolo[4,5-g]isoquinoline-5(6H),7'-[7H]indeno[4,5-d][1,3]dioxole]-6',8'-diol;d-Ochrobirine;Ochrobirine
• CAS NO: 24181-64-4
• Molecular Formula: C20H19 N O6
• Molecular Weight: 369.37
• Mol File: 24181-64-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Ochrobirine(CAS DataBase Reference)
• NIST Chemistry Reference: Ochrobirine(24181-64-4)
• EPA Substance Registry System: Ochrobirine(24181-64-4)

Safety Data

• Hazardous Substances Data: 24181-64-4(Hazardous Substances Data)

Usage

Description

Ochrobirine is a Corydalis alkaloid derived from various Corydalis plant species, including C. lutea, C. ochroleuca, and C. sibirica. It forms colorless crystals and has a specific melting point and optical rotation. The structure of the alkaloid has been confirmed through chemical, physical evidence, and the synthesis of its optically active form.

Uses

1. Used in Pharmaceutical Industry:
Ochrobirine is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: Ochrobirine is used as a pharmaceutical compound for its potential therapeutic applications.
2. Used in Chemical Research:
Ochrobirine is used as a subject of study in chemical research to understand its properties, structure, and potential interactions with other compounds. The expression is: Ochrobirine is used as a subject of study in chemical research for understanding its properties, structure, and potential interactions with other compounds.
3. Used in Synthesis of Optically Active Forms:
Ochrobirine is used in the synthesis of its optically active form, which can be beneficial for various applications in the pharmaceutical and chemical industries. The expression is: Ochrobirine is used in the synthesis of its optically active form for potential applications in the pharmaceutical and chemical industries.

References

Manske., Can. J. Res., 18B, 75 (1940)Total synthesis: Kametani, Hibino, Takano., Chern. Cornrnun., 925 (1971)

Upstream product

• 99132-03-3 C₂₀H₁₅NO₆ 
• 99132-04-4 C₂₁H₁₉NO₇ 
• 99132-05-5 C₂₁H₂₁NO₇ 
• 96860-74-1 Protoberberine 
• 24181-66-6 (+/-)-sibiricine 
• 84229-86-7 C₁₉H₁₃NO₅ 
• 3486-66-6 coptisine 
• 2086-83-1 berberine 
• 50506-18-8 8t-bromo-2'-formyl-6',7'-bis-methoxycarbonyloxy-3',4'-dihydro-8H,2'H-(7rN)-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-6-one 
• 50506-19-9 2'-formyl-8c-hydroxy-6',7'-bis-methoxycarbonyloxy-3',4'-dihydro-8H,2'H-(7rN)-spiro[indeno[4,5-d][1,3]dioxole-7,1'-isoquinolin]-6-one 
• 38699-86-4 5-bromo-indeno[4,5-d][1,3]dioxole-6,7,8-trione 7-hydrate 
• 38699-87-5 5'-bromo-7,8-dihydro-6H-spiro[[1,3]dioxolo[4,5-g]isoquinoline-5,7'-indeno[4,5-d][1,3]dioxole]-6',8'-dione 
• 1484-85-1 3,4-methylenedioxyphenylethylamine 
• 33742-75-5 indeno[4,5-d][1,3]dioxole-6,7,8-trione 8-hydrate 

Relevant articles and documents

A NOVEL AND HIGHLY STEREOSELECTIVE SYNTHESIS OF (+/-)-SIBIRICINE

A novel and stereoselective synthesis of (+/-)-sibiricine (1), a spirobenzylisoquinoline alkaloid, from the corresponding protoberberine (3) was developed using photo-oxygenation and photo-isomerization.

STRUCTURE OF LEDERINE

The new spirobenzylisoquinoline base lederine with mp 208-209 deg C (methanol), D +13 deg (c 0.84; chloroform) has been isolated from Corydalis ledebouriana Kar et Kir and Dicentra peregrina (Rudolphi) Fedde.Its structure has been established om the basis of spectral characteristics and chemical reactions.