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126170-40-9

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126170-40-9 Usage

Description

[(2S,4R)-4-(6-amino-9H-purin-9-yl)oxetan-2-yl]methanol, commonly known as adenosine, is a nucleoside that plays a vital role in various biological processes. It is composed of a purine base (adenine) connected to a ribose sugar molecule, with a methyl group and hydroxyl group attached to the ribose. Adenosine is crucial for cellular energy transfer as it is a component of ATP (adenosine triphosphate) and ADP (adenosine diphosphate). Additionally, it functions as a neurotransmitter, regulating blood flow, heart function, and neurotransmitter release.

Uses

Used in Pharmaceutical Applications:
Adenosine is utilized as a drug for treating specific heart conditions, such as supraventricular tachycardia and atrial fibrillation. It helps in regulating the heart rate and maintaining a stable rhythm.
Used in Diagnostic Applications:
Adenosine is also employed as a diagnostic agent for heart imaging, particularly in stress tests and nuclear medicine imaging. It aids in the visualization of the heart's blood flow and function, allowing for the detection of potential issues.
Used in Cellular Energy Transfer:
Adenosine plays a critical role in cellular energy transfer as a component of ATP and ADP, which are essential for various cellular processes and energy production.
Used in Neurotransmission:
Adenosine functions as a neurotransmitter, regulating blood flow, heart function, and neurotransmitter release, contributing to the overall maintenance of the body's homeostasis.
Used in Research and Development:
Adenosine is also used in research and development for studying the mechanisms of cellular energy transfer, neurotransmission, and the development of new drugs targeting these processes.

Check Digit Verification of cas no

The CAS Registry Mumber 126170-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,7 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126170-40:
(8*1)+(7*2)+(6*6)+(5*1)+(4*7)+(3*0)+(2*4)+(1*0)=99
99 % 10 = 9
So 126170-40-9 is a valid CAS Registry Number.

126170-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,4R)-4-(6-aminopurin-9-yl)oxetan-2-yl]methanol

1.2 Other means of identification

Product number -
Other names 9-((2R,4S)-4-(Hydroxymethyl)-2-oxetanyl)adenine

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:126170-40-9 SDS

126170-40-9Downstream Products

126170-40-9Relevant articles and documents

Reducing dehalogenating method of organic halogenated compound

-

Paragraph 0099; 0100; 0102; 0124; 0129; 0132, (2019/02/10)

The invention discloses a reducing dehalogenating method of an organic halogenated compound. The reducing dehalogenating method comprises: mixing an organic halogenated compound R-X, a non-noble metalpromoter, a sulfide and an alkali, and carrying out a reducing dehalogenating reaction to obtain a reducing product R-H, wherein R is at least one selected from alkyl and aryl, and X is at least oneselected from iodine, bromine and chlorine. According to the present invention, the types and the ratio (especially the specific type of the promoter) of various raw materials used in the reducing dehalogenating reaction, the corresponding reaction conditions and the like are researched and improved, such that the problems of use of highly-toxic or expensive reagent, poor tolerance of the group, narrow application range of the substrate and the like in the prior art can be effectively solved.

Synthesis and antiviral activity of oxetanocin derivatives

Kitagawa, Masayuki,Hasegawa, Shigeru,Saito, Seiichi,Shimada, Nobuyoshi,Takita, Tomohisa

, p. 3531 - 3534 (2007/10/02)

The sugar part of natural oxetanocin A was chemically modified. Some of the derivatives demonstrated strong antiviral activity against human immunodeficiency virus (HIV).

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