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1-(6-amino-7H-purin-7-yl)-3-[(2-hydroxyethyl)(propan-2-yl)amino]propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65551-71-5

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65551-71-5 Usage

Chemical class

Purine derivative

Explanation

The compound is a derivative of purine, a heterocyclic aromatic organic compound.

Explanation

The compound has a purine base, which is similar to adenine and guanine, essential components of DNA and RNA.

Explanation

Due to its unique structure and properties, the compound may have potential implications in medicinal chemistry, particularly in the development of pharmaceutical drugs.

Explanation

The precise biological and chemical properties of the compound would need to be further studied and characterized to understand its potential applications fully.

Explanation

The molecular formula represents the number of atoms of each element present in the compound, which is essential for understanding its structure and properties.

Explanation

The solubility of the compound is not mentioned in the provided material, and further research would be needed to determine its solubility in various solvents.

Explanation

The stability of the compound under different conditions is not provided in the material, and further research would be needed to determine its stability.

Explanation

The reactivity of the compound with other substances is not mentioned in the material, and further research would be needed to understand its reactivity profile.

Explanation

The toxicity of the compound is not provided in the material, and further research would be needed to determine its potential toxic effects on living organisms.

Structural components

Hydroxyethyl group and propan-2-ylamino group

Purine base

Similar to adenine and guanine

Potential applications

Medicinal chemistry and pharmaceutical drug development

Further research needed

Biological and chemical properties

Solubility

Unknown

Stability

Unknown

Reactivity

Unknown

Toxicity

Unknown

Check Digit Verification of cas no

The CAS Registry Mumber 65551-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,5 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65551-71:
(7*6)+(6*5)+(5*5)+(4*5)+(3*1)+(2*7)+(1*1)=135
135 % 10 = 5
So 65551-71-5 is a valid CAS Registry Number.

65551-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-aminopurin-7-yl)-3-[2-hydroxyethyl(propan-2-yl)amino]propan-2-ol

1.2 Other means of identification

Product number -
Other names 1-(6-amino-purin-7-yl)-3-[(2-hydroxy-ethyl)-isopropyl-amino]-propan-2-ol

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:65551-71-5 SDS

65551-71-5Downstream Products

65551-71-5Relevant academic research and scientific papers

Salts of 5-methylpyrazole-3-carboxylic acid with basically substituted adenine derivatives/Identification and lipolysis inhibitory activity

Credner,Tauscher,Jozic,Brenner

, p. 2096 - 2100 (2007/10/02)

5-Methylpyrazole-3-carboxylic acid forms salts with basically substituted adenine bases of type (4) or (5), which have significantly more lipolysis inhibitory activity than the free acid itself. The substance tested, 6-amino-9-[2-hydroxy-3-(N-methyl-N-2-hydroxyethyl)-aminopropyl]-purine-5-methylpyrazole-3-carboxylate (16), causes a significant reduction of serum FFA levels in fasted rats, even at the very low dosage of 0.150 mg/kg b.w., whereas the free 5-methyl-pyrazole-3-carboxylic-acid shows significant activity in this model only at doses of 2 mg/kg b.w. and above. The salt also shows similar activity on serum triglycerides. The effects on FFA, triglyceride and cholesterol levels, respectively, in fasted rats lasts for at least 8 h.

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