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3,3,6,6,9-pentamethyl-3,4,5,6,7,9-hexahydro-1H-xanthene-1,8(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19225-63-9

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19225-63-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19225-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19225-63:
(7*1)+(6*9)+(5*2)+(4*2)+(3*5)+(2*6)+(1*3)=109
109 % 10 = 9
So 19225-63-9 is a valid CAS Registry Number.

19225-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,6,6,9-pentamethyl-4,5,7,9-tetrahydro-2H-xanthene-1,8-dione

1.2 Other means of identification

Product number -
Other names Acetaldehyd-bismethon-anhydrid

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:19225-63-9 SDS

19225-63-9Relevant academic research and scientific papers

An efficient heterogeneous iron oxide nanoparticle catalyst for the synthesis of 9-substituted xanthene-1,8-dione

Thirumalai, Dhakshanamurthy,Gajalakshmi, Shanmugam

, p. 2657 - 2668 (2020)

Abstract: An efficient and simple method for the synthesis of xanthene derivatives by using iron oxide nanoparticles (NPs) as a catalyst has been investigated. Synthesis of 9-substituted xanthene-1,8-dione derivatives involves one-pot reaction of dimedone

Features of the Reaction of Dimedone with Some Amines in the Presence of Mercury(II) Acetate

Hobosyan,Balyan,Nersisyan,Galechyan,Sargsyan,Tamazyan,Ayvazyan

, p. 2518 - 2521 (2021/02/12)

Abstract: Regiochemistry of the reaction of N-substituted propargylamines with dimedone in the presence of mercury(II) acetate was studied. Xanthene and diene derivatives, as well as symmetric mercury aminopropinides, were obtained, for one of which the c

Tungstophosphoric acid nanoparticles supported on polyamic acid: A mild and recoverable heterogeneous catalyst for the selective synthesis of mono and bulky bis(1,8-dioxooctahydroxanthene)s under solvent-free conditions

Nasr-Esfahani, Masoud,Rafiee, Zahra,Kashi, Hassan

, p. 790 - 799 (2016/05/09)

A series of 1,8-dioxooctahydroxanthene derivatives and some crowded bis(1,8-dioxooctahdroxanthene) were selectively synthesized using tungstophosphoric acid nanoparticles supported on polyamic acid (TPA/PAA) as a new catalyst in solvent-free conditions. T

Secondary amine based ionic liquid: An efficient catalyst for solvent free one pot synthesis of xanthenes and benzoxanthenes

Das, Pranab J.,Das, Jupitara

, p. 11745 - 11752 (2015/02/19)

Ionic liquids (IL) prepared from dialkylamines and concentrated sulphuric acid were used in an operationally simple, cost effective, efficient and environmentally benign synthesis of xanthenes and benzoxanthenes. Three ILs were screened for their efficien

A green and efficient procedure for one-pot synthesis of xanthenes and acridines using silica boron-sulfuric acid nanoparticles (SBSANs) as a solid Lewis-protic acid

Khalafi-Nezhad, Ali,Panahi, Farhad,Mohammadi, Somayeh,Foroughi, Habib Ollah

, p. 189 - 200 (2013/07/26)

Silica boron-sulfuric acid nanoparticles (SBSANs) as a solid Lewis-protic acid have been found to be an efficient heterogeneous catalyst in the synthesis of xanthene and acridine derivatives. The SBSAN-catalyzed reaction between carbonyl compound (aldehyd

A synthetic entry into fused pyran derivatives through carbon transfer reactions of 1,3-oxazinanes and oxazolidines with carbon nucleophiles

Singh, Kamaljit,Singh, Jasbir,Singh, Harjit

, p. 14273 - 14280 (2007/10/03)

Acid catalysed condensations of various 2 substituted 1,3-oxazinanes 3 and 1,3-oxazolidines 4 with cyclic carbon nucleophiles viz. 5,5-dimethyl-1,3-cyclohexanedione and 1,3-cyclohexanedione furnish xanthene derivatives, whereas a Knoevenagel reaction proceeds with acyclic nucleophiles. In case of 4b and 4c, a unique synthesis of functionalised α-tetralones has emerged. Reactions of mixtures of cyclic and acyclic carbon nucleophiles with 3 provide some functionalised and partially reduced benzopyran derivatives.

On the Reaction of Vinyl Isocyanates with Enamines

Prager, Rolf H.,Were, Stephen T.

, p. 1635 - 1641 (2007/10/02)

Vinyl isocyanate reacts with enamines to give N-vinyl carboxamides which, unlike the more highly substituted analogues, do not cyclize readily to 2-pyridones.

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