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1-(3-bromophenoxy)-1-ethoxyethane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127972-99-0

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127972-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127972-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,7 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127972-99:
(8*1)+(7*2)+(6*7)+(5*9)+(4*7)+(3*2)+(2*9)+(1*9)=170
170 % 10 = 0
So 127972-99-0 is a valid CAS Registry Number.

127972-99-0Relevant articles and documents

3 - Acetoxystyrene production

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Paragraph 0028-0029, (2021/11/02)

[Problem] industrially easily available raw material can be used, or the deleterious reaction reagent, which does not require special equipment, new 3 - acetoxystyrene manufacturing method. [Solution] the following i) - iii) comprising the steps of, manuf

New Access Routes to Privileged and Chiral Ligands for Transition-Metal Catalyzed Hydrogen Autotransfer (Borrowing Hydrogen), Dehydrogenative Condensation, and Alkene Isomerization Reactions

Hintermann, Lukas,Jandl, Christian,Klein, Philippe,Koller, Sebastian,Ochmann, Lukas,P?thig, Alexander,Reinhardt, Katja,Seitz, Antonia

, (2021/11/30)

A group of transition-metal catalyzed hydrogen moving reactions, encompassing hydrogen autotransfer (HAT; also called borrowing hydrogen, BH), dehydrogenative condensation (DHC) and alkene isomerization, displays high atom economy and relies on widely ava

8-HYDROXY-SUBSTITUTED ISOCOUMARINS BY LITHIATION OF BENZENE DERIVATIVES PROMOTED BY β-FUNCTIONALISED ALKYL GROUPS. A REGIOSELECTIVE AND SIMPLE SYNTHESIS OF OOSPOLACTONE

Ramacciotti, Alessio,Fiaschi, Rita,Napolitano, Elio

, p. 111 - 114 (2007/10/02)

3-(3-hydroxyphenyl)-2-butanone (obtained in 3 steps from 3-bromophenol and 3-chloro-2-butanone) was ketalised with ethylene glycol and protected at the phenolic OH as the methoxymethyl ether.The intermediate diacetal thus obtained underwent hydrogen-metal exchange with n-butyllithium; the metallated intermediate, after carbonation, methanolysis of acetal groups and elimination of methanol, regioselectively afforded the title compound (8-hydroxy-3,4-dimethylisocoumarin).

Synthesis, Phencyclidine-like Pharmacology, and Antiischemic Potential of Meta-Subsituted 1-(1-Phenylcyclohexyl)-1,2,3,6-tetrahydropyridines

Thurkauf, Andrew,Costa, Brian de,Mattson, Mariena V.,France, Charles P.,Price, Madelon T.,et al.

, p. 2211 - 2215 (2007/10/02)

A series of 1--1,2,3,6-tetrahydropyridines were prepared by the reaction between 1-(1-cyanocyclohexyl)-1,2,3,6-tetrahydropyridine (1) and an appropriately substituted Grignard reagent.The resulting compounds were tested for their phencyc

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