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1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol is a complex organic compound characterized by its unique combination of a purine base structure, a propanol group, and an amino acid group. The purine moiety, specifically 6-amino-9H-purin-9-yl, is a nitrogenous base commonly found in DNA and RNA, while the propanol group contributes a hydroxyl functional group and a primary alcohol. Additionally, the amino acid group features a hydroxyethyl and methyl substituent. 1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol's distinctive structure and chemical properties make it a promising candidate for various applications in the fields of pharmaceuticals, biochemistry, and genetic research.

65551-69-1

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65551-69-1 Usage

Uses

Used in Pharmaceutical Applications:
1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol is used as a pharmaceutical compound for its potential therapeutic applications. The presence of the purine base structure, which is a key component of DNA and RNA, suggests that 1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol may have roles in modulating cellular processes and could be utilized in the development of novel drugs targeting genetic disorders or diseases related to nucleic acid metabolism.
Used in Biochemical Research:
In the field of biochemistry, 1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol is used as a research tool to study the interactions between nucleic acids and other biomolecules. Its unique structure allows for the investigation of various biochemical pathways and mechanisms, contributing to a deeper understanding of cellular processes and the development of targeted therapies.
Used in Genetic Research:
1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol is also utilized in genetic research for its potential applications in gene editing and manipulation. 1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol's structure, which includes a purine base and an amino acid group, may facilitate the development of new techniques for genetic engineering and the study of gene expression and regulation.
Used in Drug Delivery Systems:
Similar to gallotannin, 1-(6-amino-9H-purin-9-yl)-3-[(2-hydroxyethyl)(methyl)amino]propan-2-ol could be employed in the development of innovative drug delivery systems. Its unique chemical properties may enable the design of novel carriers for drug molecules, improving their delivery, bioavailability, and therapeutic outcomes in various medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 65551-69-1 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, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65551-69:
(7*6)+(6*5)+(5*5)+(4*5)+(3*1)+(2*6)+(1*9)=141
141 % 10 = 1
So 65551-69-1 is a valid CAS Registry Number.

65551-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-aminopurin-9-yl)-3-[2-hydroxyethyl(methyl)amino]propan-2-ol

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 -
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More Details:65551-69-1 SDS

65551-69-1Downstream Products

65551-69-1Relevant 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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