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1-BENZHYDRYL-3-ETHYLAZETIDIN-3-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147293-65-0

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147293-65-0 Usage

Psychoactive effects

Dissociative, hallucinogenic, and sedative

Chemical class

Diarylethylamines

Structural relation

Related to ketamine

Mechanism of action

Selective NMDA receptor antagonist

Medical use

Not approved

Recreational use

Primary use

Classification

Designer drug

Legal status

Illegal in many countries

Regulatory control

Subject to control measures

Potential for abuse

High

Adverse effects

Negative impact on mental and physical health

Check Digit Verification of cas no

The CAS Registry Mumber 147293-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,9 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 147293-65:
(8*1)+(7*4)+(6*7)+(5*2)+(4*9)+(3*3)+(2*6)+(1*5)=150
150 % 10 = 0
So 147293-65-0 is a valid CAS Registry Number.

147293-65-0Relevant academic research and scientific papers

N2-PHENYL-PYRIDO[3,4-D]PYRIMIDINE-2,8-DIAMINE DERIVATIVES AND THEIR USE AS MPS1 INHIBITORS

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Page/Page column 135, (2015/09/28)

The present invention relates to compounds of formula (I) wherein R1, R2, R3 and R4 are all as defined herein. The compounds of the present invention are known to inhibit the spindle checkpoint function of Monospindle 1 (Mps1 –also known as TTK) kinases either directly or indirectly via interaction with the Mps1 kinase itself. In particular, the present invention relates to the use of these compounds as therapeutic agents for the treatment and/or prevention of proliferative diseases, such as cancer. The present invention also relates to processes for the preparation of these compounds, and to pharmaceutical compositions comprising them.

TAXANE COMPOUND WITH AZETIDINE RING STRUCTURE

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Page/Page column 14-15, (2008/12/06)

A compound represented by the general formula (1) [X1 and X2 represent hydrogen atom, a halogen atom, hydroxyl group and the like, R1 represents a phenyl group, R2 represents an alkyl group, an alkenyl group, or

7-Azetidinylquinolones as antibacterial agents. Synthesis and structure- activity relationships

Frigola,Pares,Corbera,Vano,Merce,Torrens,Mas,Valenti

, p. 801 - 810 (2007/10/02)

A series of novel antibacterial quinolones and naphthyridones has been prepared which contain 7-azetidinyl substituents in place of the usual piperazine or aminopyrrolidine groups. These azetidinyl derivatives were evaluated for in vitro activity by deter

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