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Ethanone, 1-(2-amino-6-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20895-91-4

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20895-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20895-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20895-91:
(7*2)+(6*0)+(5*8)+(4*9)+(3*5)+(2*9)+(1*1)=124
124 % 10 = 4
So 20895-91-4 is a valid CAS Registry Number.

20895-91-4Relevant academic research and scientific papers

Synthesis method of 5-chloroquinoline-4-ol

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Paragraph 0036-0038; 0042-0044; 0048-0050, (2021/01/20)

The invention provides a synthesis method of 5-chloroquinoline-4-ol, and relates to the technical field of pharmaceutical synthesis. The method comprises the following steps of: reacting 2-amino-6-chlorobenzonitrile serving as a raw material with methyl m

Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands: Structure-activity relationship elucidation

Peters, Jens-Uwe,Luebbers, Thomas,Alanine, Alexander,Kolczewski, Sabine,Blasco, Francesca,Steward, Lucinda

, p. 256 - 261 (2008/12/23)

The optimisation of affinity and selectivity in a novel series of dual 5-HT5A/5-HT7 receptor ligands is described. Brain penetrant 2-aminodihydroquinazolines with low nanomolar affinities were identified.

5-Chloro-4-alkyl-3,4-dihydro-quinazolin-2-ylamine derivatives

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Page/Page column 6, (2010/11/25)

The present invention relates to compounds of formula I wherein R1, R2, R3 are as described in the specification and pharmaceutically acceptable acid addition salts and tautomers thereof. Compounds of formula I have good a

Process for the preparation of optionally substituted 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-ones

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, (2008/06/13)

A new process has been developed for the synthesis of optionally substituted 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-ones. In particular, the process is particularly adaptable for the preparation of the 5,6-disubstituted compounds, e.g., 5,6-dimethyl-1,2,3,5-tetrahydroimidazo-[2,1-b]quinazolin-2-one. The compounds so prepared are useful as blood platelet anti-aggregative and/or antihypertensive agents in mammals, including humans.

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