N-[5-Bromomethyl-4-(4-fluorophenyl)-6-isopropylpyrimidine-2-yl]-N-methylmethane sulfonamide

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Chemical Name:  N-[5-Bromomethyl-4-(4-fluorophenyl)-6-isopropylpyrimidine-2-yl]-N-methylmethane sulfonamide 
CAS.NO: 799842-07-2
Synonyms:
N-[5-(bromomethyl)-4-(4-fluorophenyl)-6-propan-2-ylpyrimidin-2-yl]-N-methylmethanesulfonamide

Molecular Formula: C16H19BrFN3O2S
Molecular Weight:  416.30800

Physical and Chemical Properties:
Density: 1.466 g/cm3
Boiling point:531.178ºC at 760 mmHg
Melting point:/
Flash point: 275.047ºC
Refractive index: 1.586

Specification:
Appearance: White to off-White  Powder
Purity:≥98.0%
Max single impurity:≤1.0%
Loss on drying:≤0.5%

Packing:
 25kg  cardboard drum or according to customer specified requirements
Storage:
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
Application: 
 Intermediates of Rosuvastatin CAS:287714-41-4.

 N-[5-Bromomethyl-4-(4-fluorophenyl)-6-isopropylpyrimidine-2-yl]-N-methylmethane sulfonamide


Related News: We are pleased to work with Inceptua, given their strong record of administering such programs successfully.”Trifluoromethanesulfonicanhydride CAS:358-23-6 It does not require a production license for the drug substance, and can be produced in an ordinary chemical plant. As long as it reaches a certain level, it can be used for the synthesis of the drug substance.1839-18-5 It does not require a production license for the drug substance, and can be produced in an ordinary chemical plant. As long as it reaches a certain level, it can be used for the synthesis of the drug substance.5-Methyl-2-pyrazinecarboxylic acid CAS:5521-55-1 “Administrative Measures for the Joint Review, Review and Approval of Raw Materials, Medicinal Auxiliaries and Pharmaceutical Packaging Materials and Pharmaceutical Preparations” (Consultation Draft) issued by the State Food and Drug Administration in December 2017. Supervision departments no longer accept applications for registration of APIs, pharmaceutical excipients, and packaging materials.“Administrative Measures for the Joint Review, Review and Approval of Raw Materials, Medicinal Auxiliaries and Pharmaceutical Packaging Materials and Pharmaceutical Preparations” (Consultation Draft) issued by the State Food and Drug Administration in December 2017. Supervision departments no longer accept applications for registration of APIs, pharmaceutical excipients, and packaging materials.

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