Name: Name:2,4-Dimethoxypyrimidine
Brand: AABLOCKS
SKU: AA003FR3
Rating: 90 (10 reviews)

Catalog No.: AA003FR3

3551-55-1 | 2,4-Dimethoxypyrimidine

Pack Size： 1g

Purity： 98%

in stock

$6.00 $4.00

Pack Size： 5g

Purity： 98%

in stock

$7.00 $5.00

Pack Size： 25g

Purity： 98%

in stock

$24.00 $17.00

Pack Size： 100g

Purity： 98%

in stock

$94.00 $66.00

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Technical Information

Catalog Number: AA003FR3

Chemical Name: 2,4-Dimethoxypyrimidine

CAS Number: 3551-55-1

Molecular Formula: C6H8N2O2

Molecular Weight: 140.1399

MDL Number: MFCD00056028

SMILES: COc1ccnc(n1)OC

Properties

BP: 241.6°C at 760 mmHg

Form: Liquid

MP: 17°C

Refractive Index: n20/D 1.502(lit.)

Storage: Keep in dry area;Room Temperature;

Complexity: 99.7

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 10

Hydrogen Bond Acceptor Count: 4

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 2

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 0.8

Literature fold

Title: Deprotonative metalation of aromatic compounds by using an amino-based lithium cuprate.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20110905

Title: Short access to 6-substituted pyrimidine derivatives by the S(RN)1 mechanism. Synthesis of 6-substituted uracils through a one-pot procedure.

Journal: The Journal of organic chemistry20100806

Title: Identification of gp96 as a novel target for treatment of autoimmune disease in mice.

Journal: PloS one20100101

Title: Quantification of atrazine, phenylurea, and sulfonylurea herbicide metabolites in urine by high-performance liquid chromatography-tandem mass spectrometry.

Journal: Journal of analytical toxicology20070501

Title: The cyclization transformation of the sulfonylurea herbicide flupyrsulfuron in the soil of winter wheat crops.

Journal: Pest management science20030801

Title: Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii.

Journal: Biochemical pharmacology19940817

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