39976-03-9

Basic information

• Product Name: ST5446612
• Synonyms: 2-(hydroxymethyl)-N-methylbenzamide;2-(hydroxymethyl)-N-methyl-benzamide;N-methyl-2-methylol-benzamide;ST5446612
• CAS NO: 39976-03-9
• Molecular Weight: 165.192
• Mol File: 39976-03-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: ST5446612(CAS DataBase Reference)
• NIST Chemistry Reference: ST5446612(39976-03-9)
• EPA Substance Registry System: ST5446612(39976-03-9)

Safety Data

• Hazardous Substances Data: 39976-03-9(Hazardous Substances Data)

Upstream product

• 87-41-2 2-benzofuran-1(3H)-one 
• 74-89-5 methylamine 
• 550-44-7 N-methylphthalimide 
• 85-44-9 phthalic anhydride 
• 137451-46-8 N-(phthalimidomethylsulphinyl)-L-phenylalanine tert-butyl ester 
• 137472-52-7 N-(phthalimidomethylsulphenyl)-L-phenylalanine tert-butyl ester 
• 136918-14-4 phthalimide 
• 2170-09-4 N,2-dimethylbenzamide 
• 137451-52-6 (S)-2-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethanesulfonylamino)-3-phenyl-propionic acid tert-butyl ester 

Downstream Products

• 211438-67-4 N-Methyl-2-(tetrahydro-pyran-2-yloxymethyl)-benzamide 
• 51802-87-0 2-methyl-1-phenyl-isoindole 
• 211438-72-1 N-Hexadecyl-N-methyl-2-(tetrahydro-pyran-2-yloxymethyl)-benzamide 
• 211438-76-5 N-Benzyl-N-methyl-2-(tetrahydro-pyran-2-yloxymethyl)-benzamide 

Relevant articles and documents

Preparation method of hydroxyamide

The invention discloses a preparation method of a hydroxyamide shown as formula (I). The hydroxyamide is prepared through homogeneous catalytic hydrogenation reaction of a cyclic imide represented byformula (II), wherein R1, R2 and R3 are respectively and

NOVEL ULK1 INHIBITORS AND METHODS USING SAME

In certain aspects, the invention provides a method for treating a disease or condition in a subject, the method comprising co-administering to a subject in need thereof a therapeutically effective amount of at least one ULK1-inhibiting pyrimidine, and a therapeutically effective amount of an mTOR inhibitor.

A new strategy for the preparation of secondary amines via o- (tetrahydropyranyloxymethyl)-benzamides

The new synthesis strategy for the preparation of secondary amines starts from N-alkyl-phthalimides which are reduced to the corresponding o- hydroxymethyl-N-alkyl-benzamides. After protection of the hydroxy group as tetrahydropyranyl ether the N-alkyl-benzamides are alkylated to o- (tetrahydropyranyloxymethyl)-N,N-dialkyl-benzamides. The deprotection of the hydroxy group and the release of the secondary amines can be achieved in execellent yields in one reaction step using aqueous acetic acid.