23662-66-0

Basic information

• Product Name: N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE
• Synonyms: N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE;Nsc157552;1-benzyl-4-Methylpyridin-1-iuM chloride;PyridiniuM,4-Methyl-1-(phenylMethyl)-, chloride (1:1);PyridiniuM, 4-Methyl-1-(phenylMethyl)-, chloride
• CAS NO: 23662-66-0
• Molecular Formula: C₁₃H₁₄N*Cl
• Molecular Weight: 219.714
• Mol File: 23662-66-0.mol
• Article Data: 5

Chemical Properties

• Melting Point: 180-183 °C
• Appearance: /
• CAS DataBase Reference: N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE(23662-66-0)
• EPA Substance Registry System: N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE(23662-66-0)

Safety Data

• Hazardous Substances Data: 23662-66-0(Hazardous Substances Data)

Usage

General Description

N-Benzyl-4-methyl-pyridinium chloride is a chemical compound with the molecular formula C14H14ClN. It is a quaternary ammonium compound that is commonly used in organic synthesis and as a phase-transfer catalyst in organic reactions. It is also used as an antiseptic and preservative in pharmaceutical and cosmetic products. N-BENZYL-4-METHYL-PYRIDINIUM CHLORIDE is known for its ability to effectively disrupt and inhibit the growth of microorganisms, making it a valuable ingredient in a variety of industrial and commercial applications. Additionally, it is considered to be relatively stable and has low toxicity, making it a safe and effective choice for use in various products and processes.

InChI:InChI=1S/C13H14N.ClH/c1-12-7-9-14(10-8-12)11-13-5-3-2-4-6-13;/h2-10H,11H2,1H3;1H/q+1;/p-1

Upstream product

• 108-89-4 picoline 
• 100-44-7 benzyl chloride 

Downstream Products

• 5191-54-8 2-benzyl-4-methyl pyridine 
• 856848-92-5 2-benzyl-4-phenethyl-pyridine 
• 32018-56-7 1-benzyl-4-methyl-1 ,2,3,6-tetrahydropyridine 
• 660403-89-4 (3R,4R)-1-Benzyl-4-methyl-piperidine-3,4-diol 
• 18164-96-0 2-benzoyl-isonicotinic acid 
• 1352317-09-9 N,N-dimethylamino-N'-benzyl-stilbazolium p-toluenesulfonate 
• 207801-06-7 N,N-dimethylamino-N'-benzyl-stilbazolium chloride 
• 384338-21-0 N-benzyl-3-hydroxy-4-methylpiperidinium toluene-4-sulfonate 
• 32018-96-5 1-benzyl-4-methyl-piperidin-3-one 
• 384338-20-9 1-benzyl-4-methylpiperidin-3-ol 

Relevant articles and documents

A supporting france for cloth as the starting material of the preparation method (by machine translation)

The invention discloses a method for supporting france for cloth starting material N - ((3 R, 4 R) - 4 - methyl - 1 - benzyl - 3 - piperidinyl) - N - methyl - 7 - paratoluene sulfonyl - 7 H - pyrrolo [2, 3 - D] pyrimidine - 4 - amine (I) synthetic method, specific steps are as follows: to 4 - methyl pyridine as the starting material, with the benzyl chloride undergo nucleophilic substitution by the 4 - methyl - 1 - phenylmethyl - pyridine hydrochloride, under the action of the sodium borohydride reduction reaction, borohydrite - oxidation reaction, hydroxy oxidation, the introduction of the reductive amination of the stereo selectivity of the two chiral center, through a readily available and inexpensive chiral acid (L - DTTA) splitting, to obtain optically pure intermediates (3 R, 4 R) - (1 - benzyl - 4 - methyl - piperidin - 3 - yl) - methylamine, and finally with the 4 - chloro pyrrolo pyrimidine condensation is obtained. The whole method raw materials are easy, simple operation, after treatment is easy, and the cost is low. (by machine translation)

Zwitterionic chromophores and macromolecules containing such chromophores

The invention disclosed relates to functionalized zwitterionic chromophores of structural formula III and III′. Wherein A is a linear or branched alkyl group having up to 20 carbon atoms and the desired functional groups, B is hydrogen, alkyl, aryl, halo, heterocyclic, alkoxy or nitro groups at 2, 3, 5 or 6 positions on the pyridine ring, C is hydrogen, aryl or a linear or branched alkyl group at 2′, 3′, 5′ or 6′ positions on the benzene ring, which has up to 70 carbon atoms and contains the desired functional group, D is a linear or branched alkyl, aryl or substituted aryl group, which has up to 70 carbon atoms and contains the desired functional group, R is C1-C4 alkyl or aryl, and m is an integer of from 0 to 4.

Pyrrolo[2,3-d]pyrimidine compounds

A compound of the formula wherein R1, R2 and R3 are as defined above, useful as inhibitors of protein kinases, such as the enzyme Janus Kinase 3.