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2-(5-AMINO-6-CHLORO-PYRIMIDIN-4-YLAMINO)-ETHANOL is a chemical compound characterized by its molecular formula C8H11ClN4O. It features an amino group and a chloro group attached to a pyrimidine ring, along with an ethanol group. 2-(5-AMINO-6-CHLORO-PYRIMIDIN-4-YLAMINO)-ETHANOL is recognized for its potential in the pharmaceutical industry and medical research, serving as a valuable intermediate in the synthesis of various pharmaceutical compounds due to its specific chemical and biological properties.

6623-88-7

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6623-88-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(5-AMINO-6-CHLORO-PYRIMIDIN-4-YLAMINO)-ETHANOL is used as an intermediate in the synthesis of pharmaceutical compounds for its ability to contribute to the development of new drugs. Its unique structure allows it to be a building block in creating molecules with specific therapeutic properties.
Used in Medical Research:
In the field of medical research, 2-(5-AMINO-6-CHLORO-PYRIMIDIN-4-YLAMINO)-ETHANOL is utilized for its potential biological activity, which may lead to the discovery of new therapeutic agents or contribute to understanding certain biological processes.
Used in Drug Development:
2-(5-AMINO-6-CHLORO-PYRIMIDIN-4-YLAMINO)-ETHANOL is employed as a component in drug development, where its chemical properties can be leveraged to create novel drug candidates with potential applications in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6623-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6623-88:
(6*6)+(5*6)+(4*2)+(3*3)+(2*8)+(1*8)=107
107 % 10 = 7
So 6623-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H9ClN4O/c7-5-4(8)6(9-1-2-12)11-3-10-5/h3,12H,1-2,8H2,(H,9,10,11)

6623-88-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(5-amino-6-chloropyrimidin-4-yl)amino]ethanol

1.2 Other means of identification

Product number -
Other names 5-Amino-6-chlor-4-<2-hydroxy-aethyl>-pyrimidin

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:6623-88-7 SDS

6623-88-7Relevant academic research and scientific papers

Synthesis and biological evaluation of ATP analogues acting at putative purinergic P2X-receptors (on the guinea pig bladder)

Howson, William,Taylor, Edwin Michael,Parsons, Michael Edward,Novelli, Riccardo,Wilczynska, Maria Aleksandra,Harris, Deborah Tracy

, p. 433 - 440 (2007/10/02)

This paper describes studies carried out on a series of ATP analogues on the guinea pig bladder, a tissue reported to possess purinergic P2X-receptors.Optimisation of the pharmacological experimental technique enabled reproducible responses to ATP to be obtained in the 0.2-100 μM concentration range and the potencies of ATP analogues relative to ATP to be accurately determined.Alterations of the three main parts of the ATP molecule, i.e., the triphosphate, ribose and base, suggest that the triphosphate group is responsible for the efficacy of the agonist, whereas the ribose and adenine moieties are associated with affinity. quantitative analysis / ATP / purinergic / P2X-receptors / guinea pig bladder

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