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102252-89-1

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102252-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102252-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,5 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102252-89:
(8*1)+(7*0)+(6*2)+(5*2)+(4*5)+(3*2)+(2*8)+(1*9)=81
81 % 10 = 1
So 102252-89-1 is a valid CAS Registry Number.

102252-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-amino-1-(4-methoxyphenyl)but-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-amino-1-(4-methoxy-phenyl)-but-2-en-1-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:102252-89-1 SDS

102252-89-1Downstream Products

102252-89-1Relevant articles and documents

Design, Synthesis, and Crystallization-Induced Emission of Boron Difluorides β-Ketoiminates

Fedorenko, Elena V.,Mirochnik, Anatolii G.,Beloliptsev, Anton Yu.,Svistunova, Irina V.,Tretyakova, Galina O.

, p. 117 - 127 (2018)

A series of new nitrogen-containing analogues of boron difluoride benzoylacetonates with hydrogen and methyl substituents at the nitrogen atom have been synthesized. A comparative study of boron difluoride β-ketoiminates and their oxygen-containing analogues by means of luminescence and IR spectroscopic methods as well as quantum chemistry simulations was also performed.

Copper-Catalyzed Reductive Ring-Cleavage of Isoxazoles: Synthesis of Fluoroalkylated Enaminones and Application for the Preparation of Celecoxib, Deracoxib, and Mavacoxib

Wan, Chao,Pang, Jian-Yu,Jiang, Wei,Zhang, Xiao-Wei,Hu, Xiang-Guo

, p. 4557 - 4566 (2021/03/01)

We have identified a new reactivity of copper/diamine catalysis for the reductive ring-cleavage of isoxazoles to yield fluoroalkylated enaminones. This protocol has the advantage of using commercially available reagents, ease of setting up, broad tolerance of functionality, and is regiospecific and free of defluorination and reduction of reducible functional groups. The utility was demonstrated by a one-step, regioselective synthesis of fluoroalkylated pyrazole-based drugs such as celecoxib, deracoxib, and mavacoxib.

NOVEL DUAL ACTION RECEPTORS ANTAGONISTS (DARA) AT THE AT1 AND ETA RECEPTORS

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Page/Page column 237-238; 242, (2010/11/28)

The present invention relates to new compounds of the formula [Chemical formula should be inserted here. Please see paper copy] wherein R1, R2, R3, and R31 are as specified herein. The invention also relates to a method for preparation thereof, as well as combinations of the new compounds with previously known agents. The invention also relates to the use of the above-mentioned compounds and combinations for the preparation of a medicament for treating hypertension of different kinds, alleviating organ damage of different kinds, treating or preventing diabetic nephropathy, treating endothelin and angiotensin mediated disorders, and treating prostate cancer.

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