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4-Bromo-2,6-dimethylpyrimidine is a chemical compound that belongs to the group of pyrimidines, which are aromatic heterocyclic organic compounds similar to pyridine. This specific compound has the molecular formula C6H7BrN2 and is characterized by the presence of a bromine atom and two methyl groups attached to a pyrimidine ring. It appears as a white to light beige crystalline powder and is often used in the field of organic synthesis, playing a significant role in the creation of various pharmaceuticals and pesticides. As with many pyrimidines, 4-Bromo-2,6-dimethylpyrimidine should be handled with care due to its potential harmful effects if ingested or inhaled.

354574-56-4

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354574-56-4 Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-2,6-dimethylpyrimidine is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of a wide range of drug molecules, making it a valuable asset in the development of new medications.
Used in Pesticide Industry:
4-Bromo-2,6-dimethylpyrimidine is used as a key component in the formulation of certain pesticides. Its chemical properties contribute to the effectiveness of these products in controlling pests and protecting crops.
Used in Organic Synthesis:
4-Bromo-2,6-dimethylpyrimidine is used as a building block in the synthesis of complex organic molecules. Its versatility in reacting with other compounds makes it an essential tool in the field of organic chemistry, facilitating the creation of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 354574-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,4,5,7 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 354574-56:
(8*3)+(7*5)+(6*4)+(5*5)+(4*7)+(3*4)+(2*5)+(1*6)=164
164 % 10 = 4
So 354574-56-4 is a valid CAS Registry Number.

354574-56-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMO-2,6-DIMETHYLPYRIMIDINE

1.2 Other means of identification

Product number -
Other names Pyrimidine,4-bromo-2,6-dimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:354574-56-4 SDS

354574-56-4Relevant academic research and scientific papers

Application of phosphonium salts to the reactions of various kinds of amides

Sugimoto, Osamu,Mori, Miho,Moriya, Keisuke,Tanji, Ken-Ichi

, p. 1112 - 1118 (2007/10/03)

The phosphonium salts 1 and 2 prepared from triphenylphosphine and N-halogenosuccinimide proved to be applicable to the conversion of amide compounds. Especially, halogenation of electron-deficient heteroaromatic alcohols with these reagents seems to be a convenient method compared to the halogenation with phosphorus oxyhalides.

A facile bromination of hydroxyheteroarenes

Kato, Yoshiaki,Okada, Shigemitsu,Tomimoto, Koji,Mase, Toshiaki

, p. 4849 - 4851 (2007/10/03)

Bromination of hydroxyheteroarenes using P2O5/Bu4NBr proceeds under mild conditions to afford high yields of various bromoheteroarenes. This procedure is successfully applied to large-scale syntheses of bromoheteroarenes.

A facile halogenation of some hydroxyheterocycles using triphenylphosphine and N-halosuccinimide

Sugimoto, Osamu,Mori, Miho,Tanji, Ken-ichi

, p. 7477 - 7478 (2007/10/03)

Some hydroxyheterocycles were halogenated to give the corresponding haloheterocycles using triphenylphosphine and N-halosuccinimide. In comparison with the usual method using phosphorus oxyhalide, the haloheterocycles were easily isolated.

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