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149819-74-9

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149819-74-9 Usage

Explanation

Different sources of media describe the Explanation of 149819-74-9 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Purine derivatives are compounds that contain a purine ring, which is a fused six-membered nitrogen-containing ring system.
3. A hydroxyl group (-OH) is a functional group consisting of an oxygen atom bonded to a hydrogen atom. In this compound, it is attached to a sulfur atom, forming a thiol group.
4. The compound is a trans isomer, meaning that the substituents (in this case, the hydroxyl group and the 2-amino-6-chloro-9H-purin-9-yl group) are on opposite sides of the ring.
5. The compound is used in pharmaceutical research due to its potential antiviral and antitumor properties, which are attributed to its purine structure and interactions with cellular processes.
6. The compound has potential as a therapeutic agent, meaning it could be used in the treatment of specific diseases, although the exact diseases are not specified in the provided material.

Purine derivative

Heterocyclic ring structure

Hydroxyl group

Attached to a sulfur atom

Trans isomer

(2S-trans)-

Pharmaceutical research

Antiviral and antitumor properties

Therapeutic agent

Potential treatment for certain diseases

Check Digit Verification of cas no

The CAS Registry Mumber 149819-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,8,1 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 149819-74:
(8*1)+(7*4)+(6*9)+(5*8)+(4*1)+(3*9)+(2*7)+(1*4)=179
179 % 10 = 9
So 149819-74-9 is a valid CAS Registry Number.

149819-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2S,5S)-5-(2-amino-6-chloropurin-9-yl)-1,3-oxathiolan-2-yl]methanol

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:149819-74-9 SDS

149819-74-9Downstream Products

149819-74-9Relevant articles and documents

Structure-Activity Relationships of β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanyl Nucleosides as Potential Anti-HIV Agents

Jeong, Lak S.,Schinazi, Raymond F.,Beach, J. Warren,Kim, Hea O.,Shanmuganathan, Kirupathevy,et al.

, p. 2627 - 2638 (2007/10/02)

The β-D-(2S,5R)- and α-D-(2S,5S)-1,3-oxathiolanylpyrimidine and -purine nucleosides with natural nucleoside configuration were synthesized and evaluated against HIV-1 in human peripheral blood mononuclear (PBM) cells.The key intermediate 14, which was uti

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