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933770-71-9

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933770-71-9 Usage

General Description

α-benzyloxymethyl-γ-lactone is a chemical compound with a benzyl group attached to a lactone ring. It is commonly used in organic synthesis as a protecting group for alcohols, allowing for selective reactions to occur without interference from other functional groups. The benzyl group can be easily removed under mild conditions, making it a versatile tool for the modification of complex molecules. α-benzyloxymethyl-γ-lactone has also been studied for its potential therapeutic applications, such as anti-inflammatory and antitumor properties. Overall, this compound plays a crucial role in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 933770-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,7,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 933770-71:
(8*9)+(7*3)+(6*3)+(5*7)+(4*7)+(3*0)+(2*7)+(1*1)=189
189 % 10 = 9
So 933770-71-9 is a valid CAS Registry Number.

933770-71-9Relevant articles and documents

HETEROCYCLIC AMIDES AS ROCK INHIBITORS

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Page/Page column 81, (2011/10/03)

The present invention relates to new kinase inhibitors of formula (I), more specifically ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In particular, the present invention relates to new ROCK inhibitors, compositions, in particular pharmaceuticals, comprising such inhibitors, and to uses of such inhibitors in the treatment and prophylaxis of disease. In addition, the invention relates to methods of treatment and use of said compounds in the manufacture of a medicament for the application to a number of therapeutic indications including sexual dysfunction, inflammatory diseases, ophthalmic diseases and Respiratory diseases.

Studies of ring-closing mode of 4-hydroxy-2-vinylidenebutanoates: 5-exo-trig versus 5-endo-dig

Kitagaki, Shinji,Shibata, Daisuke,Mukai, Chisato

, p. 1735 - 1738 (2008/02/05)

The ring-closing mode of benzyl 4-hydroxy-2-vinylidenebutanoates (5-exo-trig vs 5-endo-dig) could precisely be controlled in a highly selective manner by the proper choice of conditions (solvent and base).

Chemoenzymatic Approach to the Synthesis of the Antiviral Agents Penciclovir and Famciclovir in Isotopically Chiral Labelled Form

Sime, John T.,Barnes, Roger D.,Elson, Stephen W.,Jarvest, Richard L.,O'Toole, Kevin J.

, p. 1653 - 1658 (2007/10/02)

The antiviral agents penciclovir and famciclovir have been synthesised in isotopically chiral form.The synthesis of (+)-methyl 4-benzyloxy-2-(hydroxymethyl)butanoate 12a by use of enzymatic hydrolysis catalysed by the lipase from Candida cylindrac

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