4398-65-6

Usage

Uses

Used in Chemical Production:
2-Chloro-2-methylhexane is used as a chemical intermediate for the synthesis of other chemicals. It serves as a building block in the production of various organic compounds, such as (1,1-Dimethyl-pentyl)-benzene, which is an aromatic compound with a branched alkyl chain.
Used in Pharmaceutical Industry:
2-Chloro-2-methylhexane is also utilized as a pharmaceutical intermediate. It plays a crucial role in the development and manufacturing of various pharmaceutical products, contributing to the synthesis of active pharmaceutical ingredients (APIs) and other essential components in medications.

InChI:InChI=1/C7H15Cl/c1-4-5-6-7(2,3)8/h4-6H2,1-3H3

Upstream product

• 625-23-0 2-methylhexan-2-ol 
• 617-29-8 2-methylhexan-3-ol 
• 71-43-2 benzene 
• 7446-70-0 aluminium trichloride 
• 539-82-2 ethyl n-valerate 
• 591-78-6 n-hexan-2-one 
• 7647-01-0 hydrogenchloride 
• 75-36-5 acetyl chloride 

Downstream Products

• 590-73-8 2,2-dimethylhexane 
• 2738-19-4 2-methyl-2-hexene 
• 6094-02-6 2-methyl-1-hexene 
• 108618-85-5 (2,2-dimethyl-hexyl)-benzene 
• 15869-95-1 4,4-dimethyloctane 
• 85705-59-5 3-[4-(1,1-dimethylpentyl)-phenyl]-2-methylpropyl chloride 
• 107918-26-3 1-cyclohexyl-2,2-dimethyl-hexane 
• 1027252-38-5 1,3-Bis<<4-(1,1-dimethylpentyl)pheny>thio>-4,6-dinitrobenzene 
• 155059-91-9 4-(1,1-Dimethylpentyl)benzenesulfonyl chloride 
• 155059-92-0 4-(1,1-Dimethylpentyl)thiophenol 
• 19219-89-7 2-Methyl-2-phenylhexane 
• 625-23-0 2-methylhexan-2-ol 

Relevant academic research and scientific papers

Direct chlorination of alcohols with chlorodimethylsilane catalyzed by a gallium trichloride/tartrate system under neutral conditions

The reaction of secondary alcohols 1 with chlorodimethylsilane (HSiMe 2Cl) proceeded in the presence of a catalytic amount of GaCl 3/diethyl tartrate to give the corresponding organic chlorides 3. In the catalytic cycle, the reaction of diethyl tartrate 4a with HSiMe 2Cl 2 gives the chlorosilyl ether 5 with generation of H2. Alcohol-exchange between the formed chlorosilyl ether 5 and the substrate alcohol 1 affords alkoxychlorosilane 6, which reacts with catalytic GaCl 3 to give the chlorinated product 3. The moderate Lewis acidity of GaCl3 facilitates chlorination. Strong Lewis acids did not give product due to excessive affinity for the oxy-functionalities. Although tertiary alcohols were chlorinated by this system even in the absence of diethyl tartrate, certain alcohols that are less likely to give carbocationic species were effectively chlorinated using the GaCl3/diethyl tartrate system. The Royal Society of Chemistry.

Novel Donor 1,4-Benzothiazinophenothiazine

The synthesis of the novel organic donor 1,4-benzothiazinophenothiazine (3) via a double Cadogan-type ring closure is reported.The target molecule is characterized by a 1H NOE-spectrum and by X-ray analysis, thus confirming the "migration" of the l