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5,7,8,15-Tetrahydro-2,3-dimethoxy-6-methylbenzo[e][1,3]dioxolo[4,5-k][3]benzazecin-14(6H)-one is a complex organic compound with a molecular formula of C18H21NO5. It is a derivative of benzazecin, a tricyclic structure that features a benzene ring fused to a dioxolane ring and a pyrrolidine ring. The compound is characterized by the presence of four hydrogen atoms in a tetrahydro environment, two methoxy groups attached to the benzene ring, and a methyl group at the 6-position. The 14(6H)-one indicates the presence of a ketone group at the 14-position, which is part of a six-membered ring. 5,7,8,15-Tetrahydro-2,3-dimethoxy-6-methylbenzo[e][1,3]dioxolo[4,5-k][3]benzazecin-14(6H)-one is likely to be found in the field of organic chemistry, potentially as a pharmaceutical intermediate or a compound with specific biological activity, given its intricate structure and functional groups.

528-67-6

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528-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 528-67-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 528-67:
(5*5)+(4*2)+(3*8)+(2*6)+(1*7)=76
76 % 10 = 6
So 528-67-6 is a valid CAS Registry Number.

528-67-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethoxy-6-methyl-5,7,8,15-tetrahydrobenzo[c][1,3 ]benzodioxolo[5,6,g]azecin-14(6H)-one

1.2 Other means of identification

Product number -
Other names fagarine II

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:528-67-6 SDS

528-67-6Downstream Products

528-67-6Relevant academic research and scientific papers

TOTAL SYNTHESIS OF PSEUDO TYPE OF PROTOPINE ALKALOIDS

Orito, Kazuhiko,Kudoh, Shigekazu,Yamada, Kinji,Itoh, Mitsuomi

, p. 11 - 14 (2007/10/02)

Photolysis of the chloroacetamides (1) gave the benzazepinones (2), whose benzyl derivatives (3) were cyclized to the benz-indenoazepines (4) by treatment with phosphoryl chloride.DYe-sensitized photo-oxygenation of 4, followed by lithium aluminum hydride reduction and manganese dioxide oxidation of the products 5, led to a total synthesis of pseudoprotopine (7a) and fagarine II (7b) as well as their analogs 7c and 7d.

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