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228851-50-1

7H-Benzo[b]pyrano[3,2-h]acridin-7-one, 3,14-dihydro-6-hydroxy-3,3-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

228851-50-1

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228851-50-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 228851-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,8,8,5 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 228851-50:
(8*2)+(7*2)+(6*8)+(5*8)+(4*5)+(3*1)+(2*5)+(1*0)=151
151 % 10 = 1
So 228851-50-1 is a valid CAS Registry Number.

228851-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Hydroxy-3,3-dimethyl-7,14-dihydro-3H-benzo[b]pyrano[3,2-h]acridin-7-one

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-3,3-dimethyl-3,14-dihydro-4-oxa-14-aza-benzo[a]naphthacen-7-one

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:228851-50-1 SDS

228851-50-1Upstream product

228851-50-1Relevant articles and documents

Synthesis and cytotoxic and antitumor activity of benzo[b]pyrano[3,2- h]acridin-7-one analogues of acronycine

Costes, Nadine,Le Deit, Hervé,Michel, Sylvie,Tillequin, Fran?ois,Koch, Michel,Pfeiffer, Bruno,Renard, Pierre,Léonce, Stéphane,Guilbaud, Nicolas,Kraus-Berthier, Laurence,Pierré, Alain,Atassi, Ghanem

, p. 2395 - 2402 (2000)

Benzo[b]acronycine (6-methoxy-3,3,14-trimethyl-3,14-dihydro-7H- benzo[b]pyrano[3,2-h]acridin-7-one, 4), an acronycine analogue with an additional aromatic ring linearly fused on the natural alkaloid basic skeleton, was synthesized in three steps, starting

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