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89943-04-4

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89943-04-4 Usage

Uses

N-(2-Pyridylamino)ethanol (cas# 89943-04-4) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 89943-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,4 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89943-04:
(7*8)+(6*9)+(5*9)+(4*4)+(3*3)+(2*0)+(1*4)=184
184 % 10 = 4
So 89943-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O/c10-6-5-9-7-3-1-2-4-8-7/h1-4,10H,5-6H2,(H,8,9)

89943-04-4 Well-known Company Product Price

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  • Aldrich

  • (CBR01241)  2-(Pyridin-2-ylamino)ethanol  AldrichCPR

  • 89943-04-4

  • CBR01241-1G

  • 966.42CNY

  • Detail

89943-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(pyridin-2-ylamino)ethanol

1.2 Other means of identification

Product number -
Other names 2-pyridin-2-ylamino-ethanol

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:89943-04-4 SDS

89943-04-4Relevant articles and documents

ADENOSINE RECEPTOR BINDING COMPOUNDS

-

Paragraph 00421, (2020/02/06)

The present invention relates to pharmaceutical compounds and compositions of Formula (I) and methods of treatment using the compounds and compositions, especially for the treatment and/or prevention of a proliferation disorder, such as cancer. Compounds of Formula (I) as further described herein are shown modulators of the adenosine A2A receptor and exhibit antiproliferative activity. Accordingly, these compounds are useful to treat proliferative disorders such as cancer, and other adenosine receptor-related conditions including an inflammatory disease, renal disease, diabetes, vascular disease, lung disease, or an autoimmune disease.

Novel thermolabile protecting groups with higher stability at ambient temperature

Chmielewski, Marcin K.

supporting information; experimental part, p. 666 - 669 (2012/02/15)

Novel thermolabile hydroxyl protecting groups of increased thermostability are proposed. The stability of these groups at different temperatures ranges has been determined. The 2-pyridyl-N-(2,4-difluorobenzyl)aminoethyl unit was selected as stable at ambient temperature and very labile at increased temperature. The half-life times for the best groups were established. Application of this chemistry to the protection of different hydroxyl groups of thymidine was also demonstrated.

A mild, catalyst-free synthesis of 2-aminopyridines

Poola, Bhaskar,Choung, Wonken,Nantz, Michael H.

, p. 10798 - 10801 (2008/12/23)

Alkylation of 2-mercaptopyridine with 1,2-dibromoethane affords a cyclic dihydrothiazolopyridinium salt that can serve as a precursor of 2-aminopyridines. Its reaction with primary or secondary amines, either neat or in DMSO, under mild conditions gives the title compounds.

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