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2-Chloro-4,6-dimethoxypyrimidine, 98%, reference material|917842|13223-25-1

2-Chloro-4,6-dimethoxypyrimidine, 98%, reference material

Cat. No JK917842_100_MG
J&K Chemical

Product Information

Product Name
2-Chloro-4,6-dimethoxypyrimidine, 98%, reference material
Brand Name
J&K
Product Number
917842
CAS
13223-25-1
Molecular Formula
C6H7ClN2O2
Molecular Weight
174.58
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
5152323
IUPAC Name
2-chloro-4,6-dimethoxypyrimidine
InChI Key
PBEKEFWBLFBSGQ-UHFFFAOYSA-N
SMILES
COC1=CC(=NC(=N1)Cl)OC

Properties

Melting Point
101-105

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H319
Precautionary Statement
P270
P330
P501
P280
P301+P317
P264+P265
P305+P351+P338
P337+P317
Storage Condition
Room temperature

References Data Source From Pubchem

Revisiting a challenging p53 binding site: a diversity-optimized HEFLib reveals diverse binding modes in T-p53C-Y220C
Publication Name: RSC Medicinal Chemistry
Publication Date: 2022-12-14
DOI: 10.1039/d2md00246a

Lanthanum-Catalyzed Arylation of Arylphosphonites
Publication Name: Science of Synthesis
Publication Date: 2018

General synthesis of 4-aryloxy-6-methylpyrimidin-2-amines and their fragmentation under positive electrospray ionization
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2015-10
DOI: 10.1134/s1070428015100127

Metal Catalyzed Cross-Coupling Reactions in the Decoration of Pyrimidine, Pyridazine, and Pyrazine
Publication Name: Synthesis and Modification of Heterocycles by Metal-Catalyzed Cross-coupling Reactions
Publication Date: 2014
DOI: 10.1007/7081_2014_138

Lithiations and Grignard Reactions on Pyrimidine and Quinazoline
Publication Name: Metalation of Azines and Diazines
Publication Date: 2012
DOI: 10.1007/7081_2012_94

2-Chloro-4,6-dimethoxypyrimidine, 98%, reference material

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