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1201676-05-2

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  • 4-(4-chloro-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-yl)piperazine-1-carboxylic acid tert-butyl ester

    Cas No: 1201676-05-2

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1201676-05-2 Usage

Molecular weight

454.96 g/mol

Structure

A t-butyl ester derivative of piperazinecarboxylic acid with a pyrrolopyridine ring system

Properties

+ Potential antiviral, antifungal, and anticancer properties
+ Shows promise in the treatment of various diseases
+ An important target for further investigation in the field of medicinal chemistry and drug development

Uses

Pharmaceutical intermediate for the synthesis of various drugs

Check Digit Verification of cas no

The CAS Registry Mumber 1201676-05-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,7 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1201676-05:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*7)+(3*6)+(2*0)+(1*5)=112
112 % 10 = 2
So 1201676-05-2 is a valid CAS Registry Number.

1201676-05-2SDS

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 4-(4-chloro-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-yl)piperazine-1-carboxylic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names 4-(4-chloro-1-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-yl)-piperazine-1-carboxylic acid tert-butyl ester

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:1201676-05-2 SDS

1201676-05-2Relevant articles and documents

Identification of potent and selective amidobipyridyl inhibitors of protein kinase D

Meredith, Erik L.,Beattie, Kimberly,Burgis, Robin,Capparelli, Michael,Chapo, Joseph,Dipietro, Lucian,Gamber, Gabriel,Enyedy, Istvan,Hood, David B.,Hosagrahara, Vinayak,Jewell, Charles,Koch, Keith A.,Lee, Wendy,Lemon, Douglas D.,Mckinsey, Timothy A.,Miranda, Karl,Pagratis, Nikos,Phan, Dillon,Plato, Craig,Rao, Chang,Rozhitskaya, Olga,Soldermann, Nicolas,Springer, Clayton,Van Eis, Maurice,Vega, Richard B.,Yan, Wanlin,Zhu, Qingming,Monovich, Lauren G.

experimental part, p. 5422 - 5438 (2010/11/18)

The synthesis and biological evaluation of potent and selective PKD inhibitors are described herein. The compounds described in the present study selectively inhibit PKD among other putative HDAC kinases. The PKD inhibitors of the present study blunt phosphorylation and subsequent nuclear export of HDAC4/5 in response to diverse agonists. These compounds further establish the central role of PKD as an HDAC4/5 kinase and enhance the current understanding of cardiac myocyte signal transduction. The in vivo efficacy of a representative example compound on heart morphology is reported herein.

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