155976-13-9 Usage
Description
Boc-L-cyclopropylglycine, also known as N-Boc-2-cyclopropyl-L-glycine, is a synthetic compound with significant applications in various industries due to its unique chemical properties. It is a white to yellow solid, which makes it easily identifiable and manageable in laboratory settings.
Uses
Used in Pharmaceutical Industry:
Boc-L-cyclopropylglycine is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the creation of novel drugs with potential therapeutic benefits.
Used in Chemical Research:
In the field of chemical research, Boc-L-cyclopropylglycine serves as a valuable compound for studying the properties and reactions of cyclopropyl-containing molecules. It aids in understanding the behavior of such molecules in different chemical environments and their potential applications.
Used in Peptide Synthesis:
Boc-L-cyclopropylglycine is used as a building block in the synthesis of cyclic peptides. Its incorporation into peptide structures can lead to the development of new bioactive molecules with specific biological activities, such as antimicrobial, antiviral, or anticancer properties.
Used in Material Science:
In material science, Boc-L-cyclopropylglycine can be utilized in the development of novel polymers and materials with unique properties. Its cyclopropyl group may impart specific characteristics to the resulting materials, making them suitable for various applications, such as in coatings, adhesives, or plastics.
Used in Agricultural Chemistry:
Boc-L-cyclopropylglycine may also find applications in agricultural chemistry, where it can be used as a precursor for the synthesis of new pesticides or herbicides. Its unique structure could potentially lead to the development of more effective and environmentally friendly products.
Check Digit Verification of cas no
The CAS Registry Mumber 155976-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,7 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155976-13:
(8*1)+(7*5)+(6*5)+(5*9)+(4*7)+(3*6)+(2*1)+(1*3)=169
169 % 10 = 9
So 155976-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO4/c1-10(2,3)15-9(14)11-7(8(12)13)6-4-5-6/h6-7H,4-5H2,1-3H3,(H,11,14)(H,12,13)
155976-13-9Relevant articles and documents
Ir-Catalyzed Enantioconvergent Synthesis of Diversely Protected Allenylic Amines Employing Ammonia Surrogates
Carreira, Erick M.,Glatz, Fabian,Petrone, David A.
supporting information, p. 16404 - 16408 (2020/07/27)
The first iridium catalyzed, enantioconvergent amination of allenylic carbonates is reported. This process utilizes various commercially available carbamates and sulfonamides to generate allenylic amines including commonly employed protected groups (Boc, Fmoc, Cbz, Ts, Ns) in 62–82 % yield and 87–98 % ee. The products generated through this scalable procedure serve as effective linchpins for the rapid, enantiospecific synthesis of a wide range of complex structures.
Preparation of (S)-1-cyclopropyl-2-methoxyethanamine by a chemoenzymatic route using leucine dehydrogenase
Parker, William L.,Hanson, Ronald L.,Goldberg, Steven L.,Tully, Thomas P.,Goswami, Animesh
experimental part, p. 464 - 469 (2012/08/08)
(S)-1-Cyclopropyl-2-methoxyethanamine is a key chiral intermediate for the synthesis of a corticotropin-releasing factor-1(CRF-1) receptor antagonist. Resolution of the racemic amine by transaminase from Vibrio fluvalis gave a 38% yield of the S-amine wit
A general, highly enantioselective method for the synthesis of D and L α-amino acids and allylic amines
Chen, Young K.,Lurain, Alice E.,Walsh, Patrick J.
, p. 12225 - 12231 (2007/10/03)
Catalytic and enantioselective synthesis of amino acids is a subject of intense interest in the field of asymmetric catalysis. Traditionally, researchers have concentrated their efforts largely on the design and discovery of enantiopure catalysts for the
