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7-Ethyl Adenine, a derivative of Adenine (A280480), is a significant compound found in animal and plant tissues. It is a constituent of nucleic acids and coenzymes, such as coenzyme I and II, adenylic acid, and coenzyme A. Its presence in various biological systems highlights its importance in cellular processes.

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  • 24309-36-2 Structure
  • Basic information

    1. Product Name: 7-Ethyl Adenine
    2. Synonyms: 7-Ethyl Adenine;7-ethylpurin-6-amine
    3. CAS NO:24309-36-2
    4. Molecular Formula: C7H9N5
    5. Molecular Weight: 163.17986
    6. EINECS: N/A
    7. Product Categories: Amines, Aromatics, Heterocycles, Nucleotides, Bases & Related Reagents, Pharmaceuticals, Intermediates & Fine Chemical
    8. Mol File: 24309-36-2.mol
  • Chemical Properties

    1. Melting Point: 237-240 °C
    2. Boiling Point: 382.2°C at 760 mmHg
    3. Flash Point: 185°C
    4. Appearance: /
    5. Density: 1.49g/cm3
    6. Vapor Pressure: 4.79E-06mmHg at 25°C
    7. Refractive Index: 1.753
    8. Storage Temp.: Refrigerator
    9. Solubility: DMSO (Slightly), Methanol (Slightly)
    10. PKA: 4.71±0.30(Predicted)
    11. CAS DataBase Reference: 7-Ethyl Adenine(CAS DataBase Reference)
    12. NIST Chemistry Reference: 7-Ethyl Adenine(24309-36-2)
    13. EPA Substance Registry System: 7-Ethyl Adenine(24309-36-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 24309-36-2(Hazardous Substances Data)

24309-36-2 Usage

Uses

Used in Pharmaceutical Industry:
7-Ethyl Adenine is used as a precursor for the preparation of alkyl bromoadenine derivatives, which serve as A2A and A2B receptor antagonists. These antagonists have potential applications in the development of drugs targeting various diseases and conditions.
Used in Microbial Determination:
7-Ethyl Adenine is utilized in the microbial determination of niacin, an essential nutrient for the human body. This application aids in understanding the role of niacin in various biological processes and its deficiency in certain conditions.
Used in Research on Heredity:
7-Ethyl Adenine plays a crucial role in research related to heredity, as it is involved in the study of genetic information and its transmission across generations. This research contributes to the understanding of genetic disorders and the development of potential treatments.
Used in Research on Virus Diseases:
In the field of virology, 7-Ethyl Adenine is used for studying virus diseases and their impact on human health. This research can lead to the development of antiviral drugs and vaccines to combat viral infections.
Used in Cancer Research:
7-Ethyl Adenine is employed in cancer research to study the mechanisms underlying tumor growth and progression. Understanding these mechanisms can help in the development of targeted therapies and improve the treatment of various types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 24309-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24309-36:
(7*2)+(6*4)+(5*3)+(4*0)+(3*9)+(2*3)+(1*6)=92
92 % 10 = 2
So 24309-36-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H9N5/c1-2-12-4-11-7-5(12)6(8)9-3-10-7/h3-4H,2H2,1H3,(H2,8,9,10)

24309-36-2SDS

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 7-ethylpurin-6-amine

1.2 Other means of identification

Product number -
Other names 7H-Purin-6-amine,7-ethyl

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:24309-36-2 SDS

24309-36-2Downstream Products

24309-36-2Relevant articles and documents

Heterocyclic Ambident Nucleophiles. III* The Alkylation of Sodium Adenide

Rasmussen, Malcolm,Hope, Janet M.

, p. 525 - 534 (2007/10/02)

The alkylation of sodium adenide in HCONMe2 (30 deg) with various alkylating agents was analysed by 1H n.m.r. spectroscopy.Widely varying N3:N7:N9 alkylation patterns were observed, depending on the alkylating agent.These patterns are interpreted in terms of the electrostatic, thermodynamic and steric factors involved in the different SN2 transition states appropriate to each alkylating agent.Hydrogen bonding association between the 6-amino group and certain carbonyl containing alkylating agents is proposed to explain the enhancedN7-alkylation in some cases.Support for this latter proposal was obtain from a comparison of the adenine alkylation results with the corresponding alkylation patterns of 6-pivaloylamino- and 6-chloro-purine.

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