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Uridine, 5-(2-bromoethenyl)-2'-deoxy-, (Z)is a modified form of uridine, a nucleoside that plays a crucial role in the synthesis of RNA and the production of neurotransmitters. This chemical compound is known for its potential therapeutic applications, particularly in the field of neuroscience. The addition of a 2-bromoethenyl group to uridine has been shown to enhance its neuroprotective and neuroregenerative properties, making it a promising candidate for the treatment of neurodegenerative diseases and traumatic brain injuries. Uridine, 5-(2-bromoethenyl)-2'-deoxy-, (Z)has also been studied for its potential in enhancing cognitive function and memory. Further research is needed to fully understand the mechanisms and potential uses of Uridine, 5-(2-bromoethenyl)-2'-deoxy-, (Z)-, but its unique properties make it an intriguing target for future drug development.

77530-02-0

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77530-02-0 Usage

Uses

Used in Pharmaceutical Industry:
Uridine, 5-(2-bromoethenyl)-2'-deoxy-, (Z)is used as a neuroprotective and neuroregenerative agent for the treatment of neurodegenerative diseases and traumatic brain injuries. Its enhanced properties make it a promising candidate for developing new therapeutic approaches to combat these conditions.
Used in Cognitive Function and Memory Enhancement:
Uridine, 5-(2-bromoethenyl)-2'-deoxy-, (Z)is used as a cognitive enhancer to improve memory and cognitive function. Its potential in this area is currently being studied, and further research is needed to fully understand its mechanisms and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 77530-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,3 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77530-02:
(7*7)+(6*7)+(5*5)+(4*3)+(3*0)+(2*0)+(1*2)=130
130 % 10 = 0
So 77530-02-0 is a valid CAS Registry Number.

77530-02-0SDS

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 (Z)-5-(2-bromovinyl)-2'-deoxyuridine

1.2 Other means of identification

Product number -
Other names 5-((Z)-2-Bromo-vinyl)-4-hydroxy-1-((2R,4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one

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:77530-02-0 SDS

77530-02-0Upstream product

77530-02-0Downstream Products

77530-02-0Relevant academic research and scientific papers

Hydrogermylation of 5-ethynyluracil nucleosides: Formation of 5-(2-germylvinyl)uracil and 5-(2-germylacetyl)uracil nucleosides

Liang, Yong,Pitteloud, Jean-Philippe,Wnuk, Stanislaw F.

, p. 5761 - 5767 (2013)

A stereoselective radical-mediated hydrogermylation of the protected 5-ethynyluracil nucleosides with trialkyl-, triaryl,- or tris(trimethylsilyl) germanes gave (Z)-5-(2-germylvinyl)uridine, 2′-deoxyuridine, or ara-uridine as major products. Reaction of the β-triphenylgermyl vinyl radical intermediate with oxygen and fragmentation of the resulting peroxyradical provided also 5-[2-(triphenylgermyl)acetyl]pyrimidine nucleosides in low to moderate yields. Thermal isomerization of the latter in MeOH occurred via a four-centered activated complex, and subsequent hydrolysis of the resulting O-germyl substituted enol yielded 5-acetyluracil nucleosides in quantitative yield.

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