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Bromohydrate du glycinate de benzoylmethyle, also known as benzoylmethyl glycinate hydrobromide, is a chemical compound with the molecular formula C10H12BrNO3. It is a white crystalline solid that is soluble in water and ethanol. bromohydrate du glycinate de benzoylmethyle is primarily used as a pharmaceutical intermediate in the synthesis of various drugs, particularly in the production of benzodiazepines, a class of psychoactive drugs used to treat anxiety, insomnia, and other conditions. The hydrobromide salt form of benzoylmethyl glycinate is often preferred due to its increased solubility and stability compared to the free base. In summary, bromohydrate du glycinate de benzoylmethyle is an important chemical intermediate in the pharmaceutical industry, playing a crucial role in the synthesis of various therapeutic agents.

6479-52-3

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6479-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6479-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,7 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6479-52:
(6*6)+(5*4)+(4*7)+(3*9)+(2*5)+(1*2)=123
123 % 10 = 3
So 6479-52-3 is a valid CAS Registry Number.

6479-52-3Relevant articles and documents

Etude de la stereochimie de la reaction de cycloaddition dipolaire-1,3 de quelques 5-phenyl-3,6-dihydro-2H-1,4-oxazin-2-ones avec les N-methyl et N-phenylmaleimides

Monnier, Karin,Schmitt, Gerard,Laude, Bernard,Mercier, Marie-France,Kubicki, Marek M.,Jannin, Michel

, p. 181 - 190 (2007/10/02)

Six derivatives of 5-phenyl-3,4-dihydro-2H-1,4-oxazin-2-ones 1 were synthetized from α-amino acids.These compounds are precursors of six-membered cyclic azomethine ylids involving one stereocenter.The 1,3-dipolar species react with N-methyl and N-phenylma

APPROACHES TO NOVEL WATER SOLUBLE PRODRUGS OF ERYTHROMYCIN A. SYNTHESIS OF 2'-O-(N-ALKYLSUCCINAMOYL)ERYTHROMYCIN DERIVATIVES INCORPORATING ANIONIC AND CATIONIC GROUPS

Ackland, Mark J.,Atkins, Paul J.,Jones, Norman B.

, p. 1265 - 1278 (2007/10/02)

Two approaches to the synthesis of 2'-O-(N-alkylsuccinamoyl)erythromycin derivatives are explored as a means of introducing anionic and cationic functionalities into erythromycin at the 2'-O-position.The phenacyl group was used to protect the anionic func

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