4409-84-1

Basic information

• Product Name: 2-deuteriotoluene
• Synonyms: 2-deuteriotoluene
• CAS NO: 4409-84-1
• Molecular Weight: 93.1326
• Mol File: 4409-84-1.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 2-deuteriotoluene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-deuteriotoluene(4409-84-1)
• EPA Substance Registry System: 2-deuteriotoluene(4409-84-1)

Safety Data

• Hazardous Substances Data: 4409-84-1(Hazardous Substances Data)

Upstream product

• 932-31-0 ortho-tolylmagnesium bromide 
• 758-12-3 deuteroacetic acid 
• 811-98-3 d⁽⁴⁾-methanol 
• 108-88-3 toluene 
• 599-00-8 trifluoroacetic acid-d₁ 
• 91996-53-1 l'alcool benzylique o-deuterie 
• 95-46-5 2-methylphenyl bromide 
• 6699-93-0 (2-methylphenyl)lithium 

Downstream Products

• 4551-39-7 2-deuteriobenzoic acid 
• 116569-21-2 <2-D₁>Benzylchlorid 
• 66154-03-8 2-deuteriobenzaldehyde 
• 857001-55-9 1-bromomethyl-2-deuterio-benzene 
• 50535-19-8 2-deuterobenzylidenedichloride 
• 108-88-3 toluene 
• 90625-40-4 trans-2,2'-dideuterio-stilbene 
• 91996-53-1 l'alcool benzylique o-deuterie 
• 43019-96-1 d₂-benzoyl chloride 
• 1311147-09-7 N-benzyl-N-(1-methoxy-2,2-dimethylpropyl)-o-deuteriobenzamide 
• 1311147-16-6 2-benzyl-3-tert-butylisoindolin-1-one 
• 1311147-24-6 2-benzyl-3-tert-butyl-7-deuterioisoindolin-1-one 
• 1443788-15-5 2-deuterio-N-(8-quinolinyl)benzamide 

Relevant articles and documents

Nickel-mediated C(sp2)-H amidation in synthesis of secondary sulfonamides via sulfonyl azides as amino source

In this paper, Ni(II)- Catalyzed ortho-amidation of C(sp2)-H bond with sulfonyl azides directed by (quinolin-8-yl) amine (AQ-amine) is described. The method provides a straightforward method for the synthesis of sulfonamides from available sulfonyl azides via the transition-metal-catalyzed C(sp2)-N bond forming reaction. The amidation reactions exhibit high functional group compatibility, which might proceed a Ni(III)/Ni(I) catalytic cycle. We also applied sulfonamide compound in OLEDs, which exhibits the certain application potential in OLEDs field.

Divergence between organometallic and single-electron-transfer mechanisms in copper(II)-mediated aerobic c-h oxidation

Copper(II)-mediated C-H oxidation is the subject of extensive interest in synthetic chemistry, but the mechanisms of many of these reactions are poorly understood. Here, we observe different products from CuII-mediated oxidation of N-(8-quinoli

USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION

A one-step method for efficiently converting carbon-hydrogen bonds into carbon-carbon bonds using chloroarenes and palladium catalysts is disclosed. This method allows faster introduction of complex molecular entities, a process that would otherwise require many more steps. This invention is particularly relevant for the organic synthesis of complex molecules such as, but not limited to, pharmacophores.