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73101-12-9

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73101-12-9 Usage

Description

(R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine is a chiral glycine derivative with a specific stereochemistry, denoted by the prefix (R)-(-). It features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to prevent unwanted reactions. (R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine also contains a 3,4-(methylenedioxy)phenyl group, indicating the presence of a methylenedioxy bridge between two phenyl rings. This chemical compound holds potential applications in various fields, including organic synthesis, peptidomimetics, pharmaceuticals, and medicinal chemistry for the development of new bioactive molecules. Its unique stereochemistry and functional groups make it a valuable building block for synthesizing complex molecules.

Uses

Used in Organic Synthesis:
(R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine is used as a chiral building block for the synthesis of complex organic molecules, taking advantage of its specific stereochemistry and functional groups.
Used in Peptidomimetics:
In the field of peptidomimetics, (R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine is used as a key component in the development of peptide-like molecules with improved stability and bioavailability.
Used in Pharmaceutical Industry:
(R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Medicinal Chemistry:
In medicinal chemistry, (R)-(-)-N-(tert-butoxycarbonyl)-3,4-(methylenedioxy)phenylglycine is used as a starting material for the design and synthesis of novel bioactive molecules, targeting specific biological pathways and receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 73101-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,0 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73101-12:
(7*7)+(6*3)+(5*1)+(4*0)+(3*1)+(2*1)+(1*2)=79
79 % 10 = 9
So 73101-12-9 is a valid CAS Registry Number.

73101-12-9Relevant articles and documents

Orally Active Cephalosporins and Penicillins

Boehme, E. H. W.,Bambury, R. E.,Baumann, R. J.,Erickson, R. C.,Harrison, B. L.,et al.

, p. 405 - 412 (2007/10/02)

A number of orally active cephalosporins and penicillins with interesting biological activity were synthesized.Two of these, 7-glycyl>amino>deacetoxycephalosporanic acid and 7-amino>deacetoxycephalosporanic acid were considerably more active than cephalexin both in vitro and in vivo against staphylococcal and streptococcal infections.

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