N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester-d6

Product Name N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester-d6
CAT No. CS-T-88729
CAS No. 1356382-52-9
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys CC(=O)NC(CSSCC(C(=O)OC(C)(C)C)NC(=O)C)C(=O)OC(C)(C)C
Canonical Smiles CC(=O)NC(CSSCC(C(=O)OC(C)(C)C)NC(=O)C)C(=O)OC(C)(C)C
InchIKey CJMDURFWZHENFZ-UIPMZEIASA-N
Inchl InChI=1S/C18H32N2O6S2/c1-11(21)19-13(15(23)25-17(3,4)5)9-27-28-10-14(20-12(2)22)16(24)26-18(6,7)8/h13-14H,9-10H2,1-8H3,(H,19,21)(H,20,22)/t13-,14-/m0/s1/i1D3,2D3
IUPAC tert-butyl (2R)-3-[[(2R)-3-[(2-methylpropan-2-yl)oxy]-3-oxo-2-[(2,2,2-trideuterioacetyl)amino]propyl]disulfanyl]-2-[(2,2,2-trideuterioacetyl)amino]propanoate
Controlled No
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N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester-d6 is a deuterated derivative of N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester. It is a chemical compound that is used in various research and analytical applications, particularly in the field of drug discovery and development. N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester-d6 is a stable and non-reactive compound that possesses a molecular weight of 426.6 g/mol. It is a deuterated derivative of N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester, which means that it contains six deuterium atoms instead of hydrogen atoms. This makes it useful in various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy where it can be used as a reference standard. The compound is also used as a starting material for the synthesis of other compounds, particularly those that are used in drug development. It is a derivative of L-cystine, an amino acid that is important in the formation of proteins. The compound is synthesized by reacting L-cystine with acetic anhydride and tert-butyl alcohol in the presence of a catalyst. Overall, N,N’-Diacetyl-L-cystine Bis(tert-Butyl) Diester-d6 is a valuable compound that is used in various research and analytical applications. Its stable and non-reactive properties, as well as its deuterated form, make it a useful tool in drug development and other scientific studies.

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