(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid
- CAS No.: 89771-75-5
- Purity: 99%
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1.What is the (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid ?
(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is a cyclohexene derivative featuring a complex structure with carboxylic acid, hydroxy, and phosphonooxy functional groups. (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid's IUPAC name reflects its stereochemistry, with the (3R,4S,5R) designation indicating the three stereocenters. The presence of these functional groups and its unique structure suggests potential applications in various fields, including pharmaceuticals, organic synthesis, and chemical research.
Used in Pharmaceutical Industry:
(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is used as a pharmaceutical compound for its potential therapeutic properties. The carboxylic acid, hydroxy, and phosphonooxy groups may allow for interactions with biological targets, offering opportunities for drug development and treatment of various diseases.
Used in Organic Synthesis:
In the field of organic synthesis, (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid serves as a versatile building block. Its functional groups can be further modified or used as a starting material for the synthesis of more complex organic molecules, contributing to the development of new chemical entities.
Used in Chemical Research:
(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is utilized in chemical research to study its properties, reactivity, and potential applications. (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid's unique structure and functional groups provide a basis for investigating new reactions, mechanisms, and the development of novel synthetic methods.
2.What is the CAS number for (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid ?
The CAS number of (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is 89771-75-5.
More information of (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid 89771-75-5 are:
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CAS?Number |
89771-75-5 |
|
Density |
1.75g/cm3 |
|
Boiling Point |
724°Cat760mmHg |
|
Flash Point |
391.6°C |
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Vapor Pressure |
3.34E-24mmHg at 25°C |
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Refractive Index |
1.602 |
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PSA |
180.63000 |
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LogP |
-0.77660 |
3.What is the molecular formula of (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid ?
The chemical formula of?(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is C10H13O10P which containing 10 Carbon atoms,13 Hydrogen atoms,10 Oxygen atoms and 1 Phosphorus atoms,and the molecular weight, and the molecular weight of (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is 324.181
4.What is (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid(89771-75-5)used for?
(3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid is a cyclohexene derivative featuring a complex structure with carboxylic acid, hydroxy, and phosphonooxy functional groups. (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid's IUPAC name reflects its stereochemistry, with the (3R,4S,5R) designation indicating the three stereocenters. The presence of these functional groups and its unique structure suggests potential applications in various fields, including pharmaceuticals, organic synthesis, and chemical research.
Relevant articles related to (3R,4S,5R)-5-[(1-carboxyethenyl)oxy]-4-hydroxy-3-(phosphonooxy)cyclohex-1-ene-1-carboxylic acid:
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Article |
Source |
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A T42M substitution in bacterial 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) generates enzymes with increased resistance to glyphosate. |
He, Ming,Nie, Yan-Fang,Xu, Peilin , p. 1405 - 1409 (2007/10/03) |
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