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2,4,5,6-Tetraaminopyrimidine, 97%|284623|1004-74-6

2,4,5,6-Tetraaminopyrimidine, 97%

Cat. No JK284623_1_G
J&K Chemical

Product Information

Product Name
2,4,5,6-Tetraaminopyrimidine, 97%
Brand Name
J&K
Product Number
284623
CAS
1004-74-6
Molecular Formula
C4H8N6
Molecular Weight
140.15
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
70487
IUPAC Name
pyrimidine-2,4,5,6-tetramine
InChI Key
PZRKPUQWIFJRKZ-UHFFFAOYSA-N
SMILES
C1(=C(N=C(N=C1N)N)N)N

Safety Information

Signal Word
Warning
Hazard Statement
H302
H332
Precautionary Statement
P264
P270
P330
P501
P261
P271
P301+P317
P304+P340

References Data Source From Pubchem

Synthesis, antitumor activities and functional mechanism of purine derivatives harboring phenyl moieties through three carbon bridges
Publication Name: Medicinal Chemistry Research
Publication Date: 2023-02-24
DOI: 10.1007/s00044-023-03038-6

From the Dawn of Organic Chemistry to Astrobiology: Urea as a Foundational Component in the Origin of Nucleobases and Nucleotides
Publication Name: Prebiotic Chemistry and Chemical Evolution of Nucleic Acids
Publication Date: 2018
DOI: 10.1007/978-3-319-93584-3_4

The molecular diversity scope of 1,3-indandione in organic synthesis
Publication Name: Molecular Diversity
Publication Date: 2015-05-10
DOI: 10.1007/s11030-015-9589-z

Compound instability in dimethyl sulphoxide, case studies with 5-aminopyrimidines and the implications for compound storage and screening
Publication Name: Bioorganic & Medicinal Chemistry Letters
Publication Date: 2012-10-15
DOI: 10.1016/j.bmcl.2012.08.065

Synthesis of Precursors for ¹8F-Labeling of Folic Acid for PET Application
Publication Name: Synthesis
Publication Date: 2011-09-29
DOI: 10.1055/s-0030-1260247

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