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253603-61-1

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253603-61-1 Usage

General Description

2-(Pyrrolidin-3-yloxy)-pyridine is a chemical compound with the molecular formula C11H14N2O. It is a pyridine derivative that contains a pyrrolidin-3-yloxy group. 2-(Pyrrolidin-3-yloxy)-pyridine is often used as a precursor or intermediate in the synthesis of pharmaceutical compounds and agrochemicals. It has also been studied for its potential biological activities, including as a potential insect repellent and in the treatment of various medical conditions. 2-(Pyrrolidin-3-yloxy)-pyridine is classified as an organic compound and is important in the field of medicinal and synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 253603-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,6,0 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 253603-61:
(8*2)+(7*5)+(6*3)+(5*6)+(4*0)+(3*3)+(2*6)+(1*1)=121
121 % 10 = 1
So 253603-61-1 is a valid CAS Registry Number.

253603-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pyrrolidin-3-yloxypyridine

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:253603-61-1 SDS

253603-61-1Downstream Products

253603-61-1Relevant articles and documents

From a novel HTS hit to potent, selective, and orally bioavailable KDM5 inhibitors

Liang, Jun,Labadie, Sharada,Zhang, Birong,Ortwine, Daniel F.,Patel, Snahel,Vinogradova, Maia,Kiefer, James R.,Mauer, Till,Gehling, Victor S.,Harmange, Jean-Christophe,Cummings, Richard,Lai, Tommy,Liao, Jiangpeng,Zheng, Xiaoping,Liu, Yichin,Gustafson, Amy,Van der Porten, Erica,Mao, Weifeng,Liederer, Bianca M.,Deshmukh, Gauri,An, Le,Ran, Yingqing,Classon, Marie,Trojer, Patrick,Dragovich, Peter S.,Murray, Lesley

supporting information, p. 2974 - 2981 (2017/05/31)

A high-throughput screening (HTS) of the Genentech/Roche library identified a novel, uncharged scaffold as a KDM5A inhibitor. Lacking insight into the binding mode, initial attempts to improve inhibitor potency failed to improve potency, and synthesis of

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