Uridine, 5-(3-amino-1-propenyl)-2'-deoxyis a chemical compound that belongs to the nucleoside family. It is a modified form of uridine, a naturally occurring nucleoside found in RNA. Uridine, 5-(3-amino-1-propenyl)-2'-deoxyis a derivative of uridine, where an amino propenyl group is added to the 5-position of the ribose ring. Its modified structure may confer different biochemical properties compared to natural uridine, making it a valuable tool for investigating nucleoside function and drug discovery.
143908-73-0
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Basic information
- Product Name: Uridine, 5-(3-amino-1-propenyl)-2'-deoxy-
- Synonyms:
- CAS NO:143908-73-0
- Molecular Formula: C12H17N3O5
- Molecular Weight: 283.284
- EINECS: N/A
- Product Categories: N/A
- Mol File: 143908-73-0.mol
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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: Uridine, 5-(3-amino-1-propenyl)-2'-deoxy-(CAS DataBase Reference)
- NIST Chemistry Reference: Uridine, 5-(3-amino-1-propenyl)-2'-deoxy-(143908-73-0)
- EPA Substance Registry System: Uridine, 5-(3-amino-1-propenyl)-2'-deoxy-(143908-73-0)
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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: 143908-73-0(Hazardous Substances Data)
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143908-73-0 Usage
Uses
Used in Biochemical Research:Uridine, 5-(3-amino-1-propenyl)-2'-deoxyis used as a research compound for studying nucleic acid chemistry. Its unique structure allows scientists to explore the interactions and functions of nucleosides in various biological processes.
Used in Pharmaceutical Research:
Uridine, 5-(3-amino-1-propenyl)-2'-deoxyis used as a starting material in the development of nucleoside analogs for potential medicinal use. Its modified structure may offer new therapeutic opportunities in the treatment of diseases where nucleoside function is implicated.
Used in Drug Discovery:
Uridine, 5-(3-amino-1-propenyl)-2'-deoxyis used as a chemical probe in drug discovery, helping researchers understand the role of nucleosides in disease mechanisms and identify potential drug targets. Its distinct properties may lead to the development of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 143908-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,9,0 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.Calculate Digit Verification of CAS Registry Number 143908-73:
(8*1)+(7*4)+(6*3)+(5*9)+(4*0)+(3*8)+(2*7)+(1*3)=140
140 % 10 = 0
So 143908-73-0 is a valid CAS Registry Number.
143908-73-0Upstream product
143908-73-0Downstream Products
- 1417629-79-8 5-(allylamino)-5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-2'-deoxyuridine
- 1417629-78-7 5-(N-9-fluorenylmethoxycarbonylallylamido)-5'-O-(4,4'-dimethoxytrityl)-3'-O-acetyl-2'-deoxyuridine
- 1417629-95-8 5-[3-(N-benzylsulfamoyl)aminoallylamino]-3’-O-acetyl-2’-deoxyuridine
- 1417629-94-7 5-[3-(N-benzylsulfamoyl)aminoallylamino]-5’-O-(4,4’-dimethoxytrityl)-3’-O-acetyl-2’-deoxyuridine
- 1417629-93-6 5-[3,5-bis(trifluoromethylphenyl)ureidoallylamido]-3’-O-acetyl-2’-deoxyuridine
- 1417629-92-5 5-[3,5-bis(trifluoromethylphenyl)ureidoallylamido]-5’-O-(4,4’-dimethoxytrityl)-3’-O-acetyl-2’-deoxyuridine
- 1417629-91-4 C43H45N5O10
- 1417629-90-3 C64H63N5O12
- 1417629-87-8 5-[(2S,4S)-N-9-fluorenylmethoxycarbonyl-2-methoxycarbonyl-4-(3’-carbamidopropanoyl)aminopyrrolidineallyl]-5’-O-(4,4’-dimethoxytrityl)-3’-O-acetyl-2’-deoxyuridine
- 1417629-84-5 5-[(2S,4R)-N-9-fluorenylmethoxycarbonyl-2-methoxycarbonyl-4-(3’-carbamidopropanoyl)aminopyrrolidineallyl]-5’-O-(4,4’-dimethoxytrityl)-3’-O-acetyl-2’-deoxyuridine
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Uridine, 5-(3-amino-1-propenyl)-2'-deoxy-
