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2,6-Diamino-4-chloropyrimidine, 98%|286276|156-83-2

2,6-Diamino-4-chloropyrimidine, 98%

Cat. No JK286276_1_G
J&K Chemical

Product Information

Product Name
2,6-Diamino-4-chloropyrimidine, 98%
Brand Name
J&K
Product Number
286276
CAS
156-83-2
Molecular Formula
C4H5ClN4
Molecular Weight
144.56
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
4-Chloro-2,6-diaminopyrimidine
PubChem CID
67432
IUPAC Name
6-chloropyrimidine-2,4-diamine
InChI Key
QJIUMVUZDYPQRT-UHFFFAOYSA-N
SMILES
C1=C(N=C(N=C1Cl)N)N

Properties

Melting Point
198-202

Safety Information

Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Nano-CoCr2O4 Catalysts Promote the Synthesis of Diamino Pyrimidine Oxide Derivatives
Publication Name: Russian Journal of General Chemistry
Publication Date: 2022-12
DOI: 10.1134/s1070363222120271

Synthesis, Characterization and Inhibition Performance of Schiff Bases for Aluminium Corrosion in 1 M H2SO4 Solution
Publication Name: Journal of Bio- and Tribo-Corrosion
Publication Date: 2019-11-01
DOI: 10.1007/s40735-019-0291-z

Synthesis, characterization, computational and biological study of novel azabenzo[a]phenothiazine and azabenzo[b]phenoxazine heterocycles as potential antibiotic agent
Publication Name: Medicinal Chemistry Research
Publication Date: 2018-02-05
DOI: 10.1007/s00044-017-2131-3

PDEStrIAn: A Phosphodiesterase Structure and Ligand Interaction Annotated Database As a Tool for Structure-Based Drug Design
Publication Name: Journal of Medicinal Chemistry
Publication Date: 2016-03-18
DOI: 10.1021/acs.jmedchem.5b01813

Synthesis, and Fluorescence Properties of Coumarin and Benzocoumarin Derivatives Conjugated Pyrimidine Scaffolds for Biological Imaging Applications
Publication Name: Journal of Fluorescence
Publication Date: 2015-10-19
DOI: 10.1007/s10895-015-1677-z

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