(3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid is a complex organic acid with a tetrahydroindolizine derivative structure, featuring a ring of carbon and nitrogen atoms. (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid is characterized by the presence of a carboxylic group, a hydroxy group, and a ketone group, which are significant functional groups in organic chemistry. Its unique structure and functional groups suggest potential pharmaceutical or biological applications, although further research and testing are necessary to ascertain its specific uses and properties.
1445865-56-4
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Basic information
- Product Name: (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid
- Synonyms:
- CAS NO:1445865-56-4
- Molecular Formula:
- Molecular Weight: 195.175
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid(CAS DataBase Reference)
- NIST Chemistry Reference: (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid(1445865-56-4)
- EPA Substance Registry System: (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid(1445865-56-4)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1445865-56-4(Hazardous Substances Data)
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1445865-56-4 Usage
Uses
Used in Pharmaceutical Industry:(3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid is used as a potential pharmaceutical candidate for [specific applications, if any are identified in the materials] due to its unique structure and functional groups. The hydroxy and ketone groups may allow for interactions with biological targets, offering opportunities for drug development.
Used in Chemical Research:
In the field of chemical research, (3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid serves as a subject for studying the properties and reactions of tetrahydroindolizine derivatives. Its complex structure provides a basis for exploring new synthetic pathways and potential applications in various chemical processes.
Please note that without specific applications identified in the materials, the uses listed are general and based on the compound's structural features and potential in the pharmaceutical and chemical research industries. Further research would be required to pinpoint exact applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1445865-56-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,8,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.Calculate Digit Verification of CAS Registry Number 1445865-56:
(9*1)+(8*4)+(7*4)+(6*5)+(5*8)+(4*6)+(3*5)+(2*5)+(1*6)=194
194 % 10 = 4
So 1445865-56-4 is a valid CAS Registry Number.
1445865-56-4Upstream product
1445865-56-4Downstream Products
- 1445865-58-6 ethyl (3S)-7-(2-amino-5-chlorophenyl)-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylate
- 1445865-16-6 2-methyl-2-propanyl {4-chloro-2-[(3S)-3-(5-{4-[(methoxycarbonyl)amino]phenyl}-4-methyl-1H-imidazol-2-yl)-5-oxo-1,2,3,5-tetrahydro-7-indolizinyl]phenyl}carbamate
- 1445961-75-0 2-methyl-2-propanyl {4-chloro-2-[(3S)-3-(4-{4-[(methoxycarbonyl)amino]phenyl}-5-methyl-1,3-oxazol-2-yl)-5-oxo-1,2,3,5-tetrahydro-7-indolizinyl]phenyl}carbamate
- 1445863-47-7 (3S)-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-3-(5-phenyl-1H-imidazol-2-yl)-2,3-dihydro-5(1H)-indolizinone
- 1445865-87-1 2-oxo-2-phenylethyl (3S)-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-5-oxo-1,2,3,5-tetrahydro-3-indolizinecarboxylate
- 1445864-93-6 N-[6-(2-{(3S)-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-5-oxo-1,2,3,5-tetrahydro-3-indolizinyl}-4-methyl-1H-imidazol-5-yl)-3-pyridinyl]acetamide
- 1445864-65-2 (3S)-3-[5-(2-amino-4-pyridinyl)-1H-imidazol-2-yl]-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-2,3-dihydro-5(1H)-indolizinone
- 1445863-86-4 methyl [4-(2-{(3S)-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-5-oxo-1,2,3,5-tetrahydro-3-indolizinyl}-1H-imidazol-5-yl)-3-methoxyphenyl]carbamate
- 1445863-87-5 methyl [2-bromo-4-(2-{(3S)-7-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]-5-oxo1,2,3,5-tetrahydro-3-indolizinyl}-1H-imidazol-5-yl)-5-methoxyphenyl]carbamate
- 1445865-62-2 (3S)-7-(2-{[(tert-butoxy)carbonyl]amino}-5-chlorophenyl)-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid
- 1445865-61-1 ethyl (3S)-7-(2-{bis[(tert-butoxy)carbonyl]amino}-5-chlorophenyl)-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylate
- 1445865-60-0 (3S)-7-[5-chloro-2-(1H-1,2,3,4-tetrazol-1-yl)phenyl]-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid
- 1445865-59-7 (3S)-7-(2-amino-5-chlorophenyl)-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid
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(3S)-7-hydroxy-5-oxo-1,2,3,5-tetrahydroindolizine-3-carboxylic acid
