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1-Piperidinecarboxylic acid, 4-(3-chloro-4-cyanophenoxy)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

583880-66-4

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583880-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 583880-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,3,8,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 583880-66:
(8*5)+(7*8)+(6*3)+(5*8)+(4*8)+(3*0)+(2*6)+(1*6)=204
204 % 10 = 4
So 583880-66-4 is a valid CAS Registry Number.

583880-66-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-[(1-tert-butoxycarbonyl-4-piperidinyl)oxy]benzonitrile

1.2 Other means of identification

Product number -
Other names -

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:583880-66-4 SDS

583880-66-4Relevant academic research and scientific papers

Discovery of ARD-2585 as an Exceptionally Potent and Orally Active PROTAC Degrader of Androgen Receptor for the Treatment of Advanced Prostate Cancer

Han, Xin,He, Miao,Kirchhoff, Paul D.,Matvekas, Aleksas,McEachern, Donna,Metwally, Hoda,Miao, Bukeyan,Qin, Chong,Sun, Duxin,Wang, Lu,Wang, Shaomeng,Wang, Yu,Wen, Bo,Xiang, Weiguo,Zhao, Lijie

, p. 13487 - 13509 (2021/09/20)

We report herein the discovery of exceptionally potent and orally bioavailable PROTAC AR degraders with ARD-2585 being the most promising compound. ARD-2585 achieves DC50values of ≤0.1 nM in the VCaP cell line with AR gene amplification and in the LNCaP cell line carrying an AR mutation. It potently inhibits cell growth with IC50values of 1.5 and 16.2 nM in the VCaP and LNCaP cell lines, respectively, and achieves excellent pharmacokinetics and 51% of oral bioavailability in mice. It is more efficacious than enzalutamide in inhibition of VCaP tumor growth and does not cause any sign of toxicity in mice. ARD-2585 is a promising AR degrader for extensive investigations for the treatment of advanced prostate cancer.

BICYCLIC BENZAMIDE COMPOUNDS AS HISTAMINE H3 RECEPTOR LIGAND USEFUL IN THE TREATMENT OF NEUROLOGICAL DISEASES

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Page 19, (2008/06/13)

The present invention relates to novel bicyclic benzamide derivatives having pharmacological activity, processes for their preparation, to compositions containing them and to their use in the treatment of neurological and psychiatric disorders.

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