4551-39-7

Basic information

• Product Name: 2-deuteriobenzoic acid
• Synonyms: 2-deuteriobenzoic acid
• CAS NO: 4551-39-7
• Molecular Weight: 123.115
• Mol File: 4551-39-7.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: 2-deuteriobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-deuteriobenzoic acid(4551-39-7)
• EPA Substance Registry System: 2-deuteriobenzoic acid(4551-39-7)

Safety Data

• Hazardous Substances Data: 4551-39-7(Hazardous Substances Data)

Upstream product

• 4409-84-1 2-deuteriotoluene 
• 35822-58-3 2-bromobenzaldehyde diethyl acetal 
• 66154-03-8 2-deuteriobenzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 18982-54-2 o-bromobenzyl alcohol 
• 124-38-9 carbon dioxide 
• 22069-99-4 1-bromo-2-deuterobenzene 
• 583-55-1 1-Bromo-2-iodobenzene 
• 615-36-1 2-bromoaniline 
• 932-31-0 ortho-tolylmagnesium bromide 
• 95-46-5 2-methylphenyl bromide 
• 88-67-5 2-Iodobenzoic acid 
• 88-65-3 2-bromobenzoic-acid 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 1620194-08-2 N-(2-(pyridin-2-yl)propan-2-yl)benzamide-2-d₁ 
• 69-72-7 salicylic acid 
• 1620193-44-3 2-hydroxy-N-(2-(pyridin-2-yl)propan-2-yl)benzamide 
• 1443788-15-5 2-deuterio-N-(8-quinolinyl)benzamide 
• 1380546-90-6 2-(3-butylhept-2-enyl)-6-(1-cyclohexylidene-3-hydroxypropan-2-yl)-N-methoxybenzamide 
• 1380546-89-3 2-(3-butylhept-2-enyl)-N-methoxy-6-(1-methoxy-4-propylhept-3-en-2-yl)benzamide 
• 1380546-87-1 2-(3-butylhept-2(Z)-enyl)-N-methoxy-6-(3-phenylhept-2-enyl)benzamide 

Relevant articles and documents

Complete replacement of H2 by D2 via Pd/C-catalyzed H/D exchange reaction

(Chemical Equation Presented) A general and in situ D2 gas generation method using 10% Pd/C-catalyzed H2-D2 exchange reaction in a H2-D2O system has been developed. H 2 gas sealed in a reac

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.

Water Compatible Hypophosphites- d2 Reagents: Deuteration Reaction via Deutero-deiodination in Aqueous Solution

Contrary to conventional deuteration approaches which typically entail deuterated solvents and/or moisture exclusion, an unprecedented deutero-deiodination reaction attainable in aqueous (H2O) solution is presented herein. By utilizing the stability of inorganic deuterated calcium/sodium hypophosphites against wayward H/D isotopic exchange within pH 2.5-11.7, these shelf-stable, nontoxic, cost-effective, and environmentally benign deuteration reagents mediate deuteration of a broad range alkyl and aryl iodides with ample isotopic incorporation in aqueous (H2O) solution.

Continuous-flow catalytic deuterodehalogenation carried out in propylene carbonate

A selective continuous-flow (CF) deuterodehalogenation approach is described performed in propylene carbonate, which is considered as one of the greenest solvents. Various CF technologies are known for hydrodehalogenation reactions; however, they are not