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28491-02-3

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28491-02-3 Usage

Chemical class

Pyrrolidine derivative

Physical properties

White to off-white crystalline powder, soluble in water and methanol

Common uses

Pharmaceutical intermediate for drug synthesis

Additional applications

Building block for organic chemistry synthesis

Research areas

Study of effects on central nervous system, potential medical treatments

Check Digit Verification of cas no

The CAS Registry Mumber 28491-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,9 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28491-02:
(7*2)+(6*8)+(5*4)+(4*9)+(3*1)+(2*0)+(1*2)=123
123 % 10 = 3
So 28491-02-3 is a valid CAS Registry Number.

28491-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-chlorophenoxy)pyrrolidine,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-(4-CHLOROPHENOXY)PYRROLIDINE HYDROCHLORIDE

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:28491-02-3 SDS

28491-02-3Relevant articles and documents

HETEROARYL DERIVATIVES OF FORMULA (I) AS ATF4 INHIBITORS

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Page/Page column 98-99, (2019/10/29)

The invention is directed to substituted heteroaryl derivatives. Specifically, the invention is directed to compounds according to Formula (I) wherein A, C, D, L2, L3, R1, R2, R3, R4, R 5, R6, z2, z4, z5, and z6 are as defined herein; or salts thereof. The compounds of the invention are inhibitors of the ATF4 pathway and can be useful in the treatment of cancer, pre-cancerous syndromes and diseases associated with activated unfolded protein response pathways, such as Alzheimer's disease, spinal cord injury, traumatic brain injury, ischemic stroke, stroke, diabetes, Parkinson disease, Huntington's disease, Creutzfeldt-Jakob Disease, and related prion diseases, progressive supranuclear palsy, amyotrophic lateral sclerosis, myocardial infarction, cardiovascular disease, inflammation, fibrosis, chronic and acute diseases of the liver, chronic and acute diseases of the lung, chronic and acute diseases of the kidney, chronic traumatic encephalopathy (CTE), neurodegeneration, dementia, cognitive impairment, atherosclerosis, ocular diseases, arrhythmias, in organ transplantation and in the transportation of organs for transplantation. Accordingly, the invention is further directed to pharmaceutical compositions comprising a compound of the invention. The invention is still further directed to methods of inhibiting the ATF4 pathway and treatment of disorders associated therewith using a compound of the invention or a pharmaceutical composition comprising a compound of the invention.

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