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6-(2-N-methylaminobenzoyl)-5,7-dimethoxy-2,2-dimethylchromene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79228-40-3

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79228-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79228-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,2 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79228-40:
(7*7)+(6*9)+(5*2)+(4*2)+(3*8)+(2*4)+(1*0)=153
153 % 10 = 3
So 79228-40-3 is a valid CAS Registry Number.

79228-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-N-methylaminobenzoyl)-5,7-dimethoxy-2,2-dimethylchromene

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:79228-40-3 SDS

79228-40-3Relevant academic research and scientific papers

RUTACEOUS CONSTITUENTS-13 A BIOMIMETIC SYNTHESIS OF ACRONYCINE

Adams, Joyce H.,Brown, P. Margaret,Gupta, Padma,Khan, M. Shafig,Lewis, John R.

, p. 209 - 218 (2007/10/02)

A biomimetic synthesis of the anti-tumor active alkaloid acronycine (7; R=R'=Me) has been obtained by cyclisation of 6-(2-methylaminobenzoyl)-5,7-dimethoxy-2,2-dimethylchromene (11; R=R'=Me); isoacronycine (20; R=R'=Me) was also produced.In an analogous manner the aminochromene (11; R=H, R'=Me) gave a mixture of des-N-methylacronycine (7; R=H, R'=Me) and des-N-methylisoacronycine (20; R=H, R'=Me).The aminochromenes were best synthesised by condensation of lithio-5,7-dimethoxy-2,2-dimethylchromene (22; R=Li) with N-methylisatoic anhydride (26) or with 2-methyl-3,1-benzoxazin-4-one (21).The relevance of this synthetic route to the biogenesis of acridone alkaloids is discussed.

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