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6247-73-0

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6247-73-0 Usage

Description

5-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-3-methyl-5-oxopent-3-enoic acid is a complex organic compound with a unique chemical structure. It is characterized by its multiple functional groups, including amino, hydroxy, and phosphoryl groups, which contribute to its potential reactivity and applications in various fields.

Uses

Used in Pharmaceutical Industry:
5-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-3-methyl-5-oxopent-3-enoic acid is used as a potential therapeutic agent for various diseases due to its complex structure and multiple functional groups, which may allow for interactions with specific biological targets.
Used in Chemical Research:
5-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-3-methyl-5-oxopent-3-enoic acid can be utilized in chemical research as a starting material or intermediate for the synthesis of other complex organic molecules. Its unique structure and functional groups make it an interesting candidate for further exploration and modification.
Used in Biochemical Applications:
Due to the presence of amino and phosphoryl groups, this compound may have potential applications in the field of biochemistry, where it could be used to study enzyme interactions, protein modifications, or as a component in the development of novel biochemical assays.
Used in Material Science:
The complex structure of this compound may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability or reactivity under certain conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6247-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6247-73:
(6*6)+(5*2)+(4*4)+(3*7)+(2*7)+(1*3)=100
100 % 10 = 0
So 6247-73-0 is a valid CAS Registry Number.

6247-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[2-[3-[[4-[[[5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethylsulfanyl]-3-methyl-5-oxopent-3-enoic acid

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:6247-73-0 SDS

6247-73-0Downstream Products

6247-73-0Relevant articles and documents

An alternative isovaleryl CoA biosynthetic pathway involving a previously unknown 3-methylglutaconyl CoA decarboxylase

Li, Yanyan,Luxenburger, Eva,Müller, Rolf

, p. 1304 - 1308 (2013)

Take a detour: An alternative pathway to synthesize isovaleryl coenzyme A (CoA) has recently been suggested in myxobacteria, which is highly active when leucine is limited. Each enzymatic step of this unprecedented route has now been characterized and a novel 3-methylglutaconyl CoA decarboxylase identified that has apparently evolved from CoA transferases. Copyright

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