114059-99-3

Basic information

• Product Name: 2-Aminobenzylchloride
• Synonyms: 2-Aminobenzylchloride
• CAS NO: 114059-99-3
• Molecular Formula: C₇H₈ClN
• Molecular Weight: 141.6
• Mol File: 114059-99-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Aminobenzylchloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Aminobenzylchloride(114059-99-3)
• EPA Substance Registry System: 2-Aminobenzylchloride(114059-99-3)

Safety Data

• Hazardous Substances Data: 114059-99-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-Aminobenzylchloride is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its ability to participate in a range of chemical reactions allows for the creation of different medicinal agents, contributing to the development of new drugs and therapeutics.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Aminobenzylchloride serves as a building block in the production of various agrochemicals. Its reactivity is harnessed to synthesize compounds that can be used in the development of pesticides, herbicides, and other agricultural chemicals, thereby supporting crop protection and enhancement efforts.
Used in Organic Synthesis:
2-Aminobenzylchloride is utilized as a versatile reagent in organic synthesis for creating a multitude of organic compounds. Its capacity to undergo various chemical transformations makes it instrumental in the synthesis of specialty chemicals, fine chemicals, and other complex organic molecules for a wide range of applications.

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 865-33-8 potassium methanolate 
• 387-45-1 2-chloro-6-fluorobenzaldehyde 
• 95-53-4 o-toluidine 
• 612-25-9 2-Nitrobenzyl alcohol 

Downstream Products

• 505052-84-6 2-(4-methylphenyl)-4H-3,1-benzothiazine 
• 181220-07-5 N-[2-(chloromethyl)phenyl]benzamide 
• 106747-44-8 2-[[(5-methoxy-1H-benzimidazol-2-yl)thio]methyl]benzenamine 
• 106746-79-6 2-?[[(5-(Trifluoromethyl)-1H-benzimidazol-2-yl)thio]methyl]benzenamine 
• 106746-78-5 2-(5-Ethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine 
• 106747-01-7 2-(5,6-Dimethoxy-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine 
• 106747-42-6 2-[[(4-methyl-1H-benzimidazol-2-yl)thio]methyl]benzenamine 
• 106746-76-3 2-(5-Methyl-1H-benzoimidazol-2-ylsulfanylmethyl)-phenylamine 
• 106747-43-7 2-[[(5,6-dimethyl-1H-benzimidazol-2-yl)thio]methyl]benzenamine 
• 57365-08-9 N-(2-aminobenzyl)-N-cyclohexyl-N-methylamine 
• 106747-37-9 2-(5,6-Dimethoxy-1H-benzoimidazole-2-sulfinylmethyl)-phenylamine 
• 106747-23-3 2-[[(5-ethoxy-1H-benzimidazol-2-yl)sulfinyl]-methyl]benzenamine 
• 106747-07-3 2-[[(5,6-dimethyl-1H-benzimidazol-2-yl)sulfinyl]methyl]benzenamine 
• 106747-06-2 2-[[(4-methyl-1H-benzimidazol-2-yl)sulfinyl]methyl]benzenamine 

Relevant articles and documents

Hydroxylation of Alkyl Halides with Water in Ionic Liquid: Significantly Enhanced Nucleophilicity of Water

A facile method for the nucleophilic hydroxylation of alkyl halides and mesylates with water has been developed in which the use of ionic liquid as an alternative reaction medium not only enhanced the nucleophilicity of water but also reduced the formation of elimination products predominantly formed under the conventional basic reaction conditions. For example, hydroxylation of model compound 2-(3-bromopropyl)naphthalene (1) to 2-(3-hydroxypropyl)-naphthalene (2) with water in 1-n-butyl-3-methylimidazolium tetrafluoroborate ([bmim] [BF 4]) and 1,4-dioxane proceeded selectively in high yield (94%). The reactivity of other nucleophilic oxygen sources such as alcohol, phenol, and acetic acid in an ionic liquid was also investigated.

Preparation method of bromhexine hydrochloride impurity C

The invention relates to the field of chemical pharmacy, in particular to a preparation method of bromhexine hydrochloride impurity C: N-methyl-N-cyclohexyl-2-aminobenzene methylamine. The method hasobvious advantages in the aspects of rapidness, high efficiency and economy. The prepared high-purity N-methyl-N-cyclohexyl-2-aminobenzene methylamine has important significance for the quality research of bromhexine hydrochloride. The preparation method comprises the following steps: (1) adding o-aminobenzyl alcohol into thionyl chloride in batches, reacting at room temperature, evaporating a solvent to dryness after the reaction is finished, adding a pulping solvent, pulping and filtering to obtain a compound 1; (2) adding the compound 1 into N-methylcyclohexylamine in batches, reacting at room temperature, after the reaction is finished, adding a solvent, refluxing, decolorizing with activated carbon, filtering, and evaporating filtrate to dryness to obtain an impurity C.

Preparation method of pyridine quinazoline intermediate (by machine translation)

N - alkylation reaction is firstly carried out on 3 - (hydrazinomethyl) pyridine and 2 - (chloromethyl) aniline followed by benzene ring substitution reaction to obtain 6 - (perfluoropropane -2 - yl) -3 - ((pyridin -3 - methylene) amino) -3 and 4 -dihydroquinazoline -2 (1H)-one. In this route, 2 - methylaniline benzyl chloride reaction is many, the design is carried out in the preceding step, 2 - (chloromethyl) aniline is subjected to high vacuum rectification, 95.0-97 .0% is reached, and impurities in subsequent reactions are reduced. In addition, the expensive raw material 2 - bromoheptafluoropropane is reacted in the following step, the raw material cost is reduced, and the total yield is 72.0-74 .0% (in 2 - bromoheptafluoropropane). (by machine translation)

Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from --C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, --C(O)--SR3, --NH--C(X)R4, and --C(=NR3)--XR7 ; B is --Wm --Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is --C(R3)p H(2-p) --; or when Q is C, W is selected from --C(R3)p H(2-p), --N(R3)m H(1-m)--, --S(O)p--, and --O--; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.