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2,4-Dichloro-6-methyl-5-nitropyrimidine, 98%|217073|13162-26-0

2,4-Dichloro-6-methyl-5-nitropyrimidine, 98%

Cat. No JK217073_1_G
J&K Chemical

Product Information

Product Name
2,4-Dichloro-6-methyl-5-nitropyrimidine, 98%
Brand Name
J&K
Product Number
217073
CAS
13162-26-0
Molecular Formula
C5H3Cl2N3O2
Molecular Weight
208.00
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
275294
IUPAC Name
2,4-dichloro-6-methyl-5-nitropyrimidine
InChI Key
NBCOZXBHPKSFSA-UHFFFAOYSA-N
SMILES
CC1=C(C(=NC(=N1)Cl)Cl)N+(=O)O-

Properties

Melting Point
53-54

Safety Information

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

References Data Source From Pubchem

Approaches to the Synthesis of 1,2,4-Triazolo[4,3-a]pyrimidines (Mini-Review)
Publication Name: Russian Journal of General Chemistry
Publication Date: 2025-01
DOI: 10.1134/s1070363224613322

Recent Updates on Morpholino Pyrimidine Derivatives as Promising PI3K/Akt/mTOR Inhibitors
Publication Name: Chemistry Africa
Publication Date: 2024-12-26
DOI: 10.1007/s42250-024-01163-2

Synthesis of New Derivatives of 4-Methyl-3-nitro-6H-pyrimido[2,1-b]quinazoline
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2020-02
DOI: 10.1134/s1070428020020232

Preparation of magnetically recoverable Fe3O4–graphene oxide catalyst by green method and its application for reduction of nitropyrimidine in aqueous medium
Publication Name: Research on Chemical Intermediates
Publication Date: 2018-07-30
DOI: 10.1007/s11164-018-3527-5

Substitution of Existing Substituents
Publication Name: Science of Synthesis
Publication Date: 2009

2,4-Dichloro-6-methyl-5-nitropyrimidine, 98%

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