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5090-87-9

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5090-87-9 Usage

General Description

2,3-Dihydro-3,6,9-trimethylnaphtho[1,8-bc]pyran-7,8-dione is a chemical compound with the molecular formula C17H16O3. It is a derivative of naphtho[1,8-bc]pyran-7,8-dione and is characterized by its three methyl groups attached to the naphtho[1,8-bc]pyran ring. 2,3-Dihydro-3,6,9-trimethylnaphtho[1,8-bc]pyran-7,8-dione has potential applications in organic synthesis and may serve as a building block for the development of new materials and pharmaceuticals. Its structure and properties make it a valuable tool in chemical research and drug discovery. Further studies on its reactivity and biological effects could lead to its use in various industrial and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 5090-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5090-87:
(6*5)+(5*0)+(4*9)+(3*0)+(2*8)+(1*7)=89
89 % 10 = 9
So 5090-87-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O3/c1-7-4-5-10-8(2)6-18-15-9(3)13(16)14(17)11(7)12(10)15/h4-5,8H,6H2,1-3H3

5090-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Mansonone E

1.2 Other means of identification

Product number -
Other names -

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:5090-87-9 SDS

5090-87-9Downstream Products

5090-87-9Relevant articles and documents

Total synthesis of mansonone e

Fang, Xianhe,Hu, Xiangdong

, p. 137 - 139 (2014/04/17)

The synthesis of mansonone E was completed in six steps and 34% overall yield from commercially available starting material 3-bromo-4-methyl acetophenone. The thermal ring expansion of a cyclobutenedione derivative followed by an intramolecular 1,3-alkoxy exchange provided a facile route to the 1,2-naphthoquinone tricyclic structure of mansonone E.

INTRAMOLECULAR DIELS-ALDER REACTIONS OF BENZYNES APPLICATION TO THE TOTAL SYNTHESIS OF MANSONONE E

Best, Wayne M.,Wege, Dieter

, p. 4877 - 4880 (2007/10/02)

Substituted benzynes can be trapped intramolecularly by an attached furan moiety and such a reaction has been used in the synthesis of the naturally occuring o-naphthoquinone mansonone E.

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