5-Iodouracil, 99%

Name: 5-Iodouracil, 99% | 696-07-1
Brand: J&K Chemical
SKU: JK101261_50_G
Price: 123.5 USD
Availability: OutOfStock

Cat. No JK101261_50_G

Vendor: J&K Chemical

Product Information

Product Name

5-Iodouracil, 99%

Brand Name

J&K

Product Number

101261

CAS

696-07-1

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

69672

IUPAC Name

5-iodo-1H-pyrimidine-2,4-dione

InChI Key

KSNXJLQDQOIRIP-UHFFFAOYSA-N

SMILES

C1=C(C(=O)NC(=O)N1)I

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Enzymatic Synthesis of Biologically Active 5-Substituted Analogues of 2ʹ-Deoxyuridine by Lactobacillus leichmannii Nucleoside Deoxyribosyltransferase Type II

Publication Name: Russian Journal of Bioorganic Chemistry

Publication Date: 2025-04

DOI: 10.1134/s106816202460569x

Effects of Nucleoside Modifications on mRNA Translation: Choosing the Right Modifications

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2025

DOI: 10.1007/978-1-0716-4742-4_4

RNA Nanotechnology: The Fundamentals

Publication Name: RNA Therapeutics in Human Diseases

Publication Date: 2025

DOI: 10.1007/978-981-96-3041-7_23

BindingDB in 2024: a FAIR knowledgebase of protein-small molecule binding data

Publication Name: Nucleic Acids Research

Publication Date: 2024-11-22

DOI: 10.1093/nar/gkae1075

Synthesis and Biological Properties of Hybrid Compounds Based on Nitrogen-Containing Heterocycles and 1,5-Disubstituted 3,7-Diazabicyclo[3.3.1]nonan-9-ones

Publication Name: Russian Journal of General Chemistry

Publication Date: 2024-11

DOI: 10.1134/s107036322411001x

5-Iodouracil, 99%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Enzymatic Synthesis of Biologically Active 5-Substituted Analogues of 2ʹ-Deoxyuridine by Lactobacillus leichmannii Nucleoside Deoxyribosyltransferase Type II

Effects of Nucleoside Modifications on mRNA Translation: Choosing the Right Modifications

RNA Nanotechnology: The Fundamentals

BindingDB in 2024: a FAIR knowledgebase of protein-small molecule binding data

Synthesis and Biological Properties of Hybrid Compounds Based on Nitrogen-Containing Heterocycles and 1,5-Disubstituted 3,7-Diazabicyclo[3.3.1]nonan-9-ones

5-Iodouracil, 99%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

About Us

Popular Searches

Contact

#title#

Features
Availability:
Price
Options
Actions

5-Iodouracil, 99%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Enzymatic Synthesis of Biologically Active 5-Substituted Analogues of 2ʹ-Deoxyuridine by Lactobacillus leichmannii Nucleoside Deoxyribosyltransferase Type II

Effects of Nucleoside Modifications on mRNA Translation: Choosing the Right Modifications

RNA Nanotechnology: The Fundamentals

BindingDB in 2024: a FAIR knowledgebase of protein-small molecule binding data

Synthesis and Biological Properties of Hybrid Compounds Based on Nitrogen-Containing Heterocycles and 1,5-Disubstituted 3,7-Diazabicyclo[3.3.1]nonan-9-ones

5-Iodouracil, 99%

Related Product

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

#title#

Login

Register