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1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol, also known as TAT, is a chemical compound with a heterocyclic structure that contains an amino group and a thiazole ring. It is a pentitol derivative that has been studied for its potential pharmaceutical properties, such as antiviral and antifungal activities. 1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol's unique structure suggests that it may have potential as a drug candidate for the treatment of various diseases. Further research is needed to fully understand its pharmacological properties and potential applications in the medical field.

71519-70-5

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71519-70-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as a potential drug candidate for its antiviral and antifungal properties, making it a promising compound for the development of new treatments for various diseases.
Used in Antiviral Applications:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as an antiviral agent due to its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Antifungal Applications:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as an antifungal agent for its ability to combat fungal infections and prevent the growth of fungi.
Further research is required to explore the full potential of 1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol in various applications and to optimize its use in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 71519-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,1 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71519-70:
(7*7)+(6*1)+(5*5)+(4*1)+(3*9)+(2*7)+(1*0)=125
125 % 10 = 5
So 71519-70-5 is a valid CAS Registry Number.

71519-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-amino-1,3-thiazol-5-yl)-5-(hydroxymethyl)oxolane-3,4-diol

1.2 Other means of identification

Product number -
Other names 1-amino-S,N-aminomethanylylidene-D-altro-2-thio-3,6-anhydro-1-deoxy-hept-1-enitol

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:71519-70-5 SDS

71519-70-5Downstream Products

71519-70-5Relevant academic research and scientific papers

A short and highly stereoselective synthesis of α-(2-aminothiazolyl)-C-nucleosides

Navarre, Jean-Michel,Guianvarc'h, Dominique,Farese-Di Giorgio, Audrey,Condom, Roger,Benhida, Rachid

, p. 2199 - 2202 (2007/10/03)

A short route to novel α-(2-aminothiazolyl)-C-nucleosides has been developed. The key step was the high diastereoselective reduction of the hemiacetal intermediates using L-Selectride, which afforded the corresponding R-diols in quantitative yields. These diols were converted, after C4-C1 ring closure and protecting groups cleavage, to their corresponding free α-C-nucleosides.

Efficient stereoselective synthesis of new C-nucleosides via intramolecular Mitsunobu cyclization

Benhida,Guianvarch,Fourrey,Sun

, p. 603 - 604 (2007/10/03)

We have studied the stereoselective synthesis of new C-nucleosides by heteroarylation of the protected γ-ribonolactone by means of heteroaromatic systems such as indole, thiazoles, imidazoles and benzimidazoles. We have observed that the first anion addit

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