26607-51-2 Usage
Description
N-Cbz-D-Alanine, also known as the Cbz-protected form of D-Alanine (A480995), is an amino acid derivative that plays a crucial role in the biosynthesis of peptidoglycan crosslinking sub-units for bacterial cell walls. It is commonly found in bacteria such as Streptococcus faecalis and is known to cause cytotoxic oxidative stress in brain tumor cells. N-Cbz-D-Alanine is a white to off-white solid and has various applications across different industries.
Uses
Used in Pharmaceutical Industry:
N-Cbz-D-Alanine is used as a building block for the synthesis of various pharmaceutical compounds. Its role in the biosynthesis of peptidoglycan crosslinking sub-units makes it a valuable component in the development of antibiotics targeting bacterial cell walls.
Used in Research and Development:
N-Cbz-D-Alanine serves as an essential research tool for studying the mechanisms of bacterial cell wall synthesis and the role of D-Alanine in this process. It is also used to investigate the cytotoxic effects of D-Alanine on brain tumor cells, potentially leading to the development of novel cancer treatments.
Used in Chemical Synthesis:
As a protected form of D-Alanine, N-Cbz-D-Alanine is used in chemical synthesis to produce a variety of compounds with specific functional groups. The Cbz protection allows for selective reactions, making it a versatile building block in organic chemistry.
Used in Material Science:
N-Cbz-D-Alanine can be utilized in the development of novel materials with specific properties, such as those with antimicrobial or anti-cancer activities. Its unique structure and reactivity make it a promising candidate for the creation of advanced materials with targeted applications.
Check Digit Verification of cas no
The CAS Registry Mumber 26607-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,0 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26607-51:
(7*2)+(6*6)+(5*6)+(4*0)+(3*7)+(2*5)+(1*1)=112
112 % 10 = 2
So 26607-51-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m1/s1
26607-51-2Relevant articles and documents
Synthesis method of silodosin
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Paragraph 0068; 0086-0088, (2021/07/24)
The invention discloses a synthesis method of silodosin. The synthesis method comprises the following steps of: sequentially performing amino protection, bromination and deprotection on indoline serving as a raw material; carrying out an SN2 reaction to o
A palladium nanoparticle-nanomicelle combination for the stereo-selective semihydrogenation of alkynes in water at room temperature
Slack, Eric D.,Gabriel, Christopher M.,Lipshutz, Bruce H.
supporting information, p. 14051 - 14054 (2015/02/19)
The addition of NaBH4 to Pd(OAc) 2 in water containing nanomicelles leads to the generation of H2 and Pd nanoparticles. Subsequent reduction of disubstituted alkynes affords Z-alkenes in high yields. These reactions are general, take place in water at ambient temperatures, and offer recycling of the aqueous reaction mixture along with low overall E Factors.
Regioselective double Boekelheide reaction: First synthesis of 3,6-dialkylpyrazine-2,5-dicarboxaldehydes from dl-alanine
Das, Sajal Kumar,Frey, Joseph
scheme or table, p. 3869 - 3872 (2012/08/14)
Pyrazine-2,5-dicarboxaldehyde was synthesized on a multi-gram scale by MnO2 oxidation of 2,5-bis(hydroxymethyl)pyrazine, which in turn was obtained from 2,5-dimethylpyrazine employing double Boekelheide reaction as a key step as reported previously. This reaction was subsequently utilized in a regioselective fashion as a key step to synthesize efficiently, for the first time, 3,6-di(long-chain)alkylpyrazine-2,5-dicarboxaldehydes starting from dl-alanine. These monomers are certain to have importance as electron deficient and chemically versatile components for new materials development.
