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2,4(1H,3H)-Quinolinedione, 3,3-bis(3-methyl-2-butenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21873-59-6

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21873-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21873-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,7 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21873-59:
(7*2)+(6*1)+(5*8)+(4*7)+(3*3)+(2*5)+(1*9)=116
116 % 10 = 6
So 21873-59-6 is a valid CAS Registry Number.

21873-59-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-bis(3-methylbut-2-enyl)-1H-quinoline-2,4-dione

1.2 Other means of identification

Product number -
Other names 3,3-diprenyl-1,2,3,4-tetrahydroquinolin-2,4-dione

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:21873-59-6 SDS

21873-59-6Relevant academic research and scientific papers

4-Hydroxycoumarin and related systems: Sitoselectivity of the Mitsunobu reaction with prenyl alcohols

Cravotto, Giancarlo,Nano, Gian Mario,Palmisano, Giovanni,Tagliapietra, Silvia

, p. 1351 - 1358 (2007/10/03)

The Mitsunobu reaction leads to the formation of new C-C bonds between prenyl alcohols and 1,3-dicarbonyl compounds like 4-hydroxycoumarin or its nitrogen isoster. Buchapine was obtained through a one-pot procedure from 4-hydroxy-2-quinolone and dimethylallyl alcohol.

A REVERSIBLE CLAISEN REARRANGEMENT OF 3-(3,3-DIMETHYLALLYL)-4-(3,3-DIMETHYLALLYLOXY)QUINOLIN-2-ONE; SYNTHESIS OF BUCHAPSINE AND LOSS OF ITS 1,1-DIMETHYLALLYL GROUP

Grundon, Michael F.,Ramachandran, V. N.

, p. 4253 - 4256 (2007/10/02)

Reversible Claisen rearrangement of 3-(3,3-dimethylallyl)-4-(3,3-dimethylallyloxy)quinolin-2-one (5) furnished the alkaloid, buchapsine (6), which readily lost the 1,1-dimethylallyl group; a mechanism for the cleavage reaction is proposed.

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