160347-94-4 Usage
General Description
FMOC-N-OMEGA-NITRO-D-ARGININE is a chemical compound that consists of an FMOC (9-fluorenylmethoxycarbonyl) protecting group attached to the amino group of the arginine molecule, along with a nitro group attached to the omega (terminal) nitrogen atom. FMOC-N-OMEGA-NITRO-D-ARGININE is often used in chemical synthesis and bioconjugation reactions due to its ability to selectively modify arginine residues in proteins and peptides. Additionally, the FMOC protecting group allows for easy removal under mild acidic conditions, making it a versatile tool for peptide and protein modification. The nitro group on the terminal nitrogen atom can also confer unique chemical reactivity and properties to the modified molecule. Overall, FMOC-N-OMEGA-NITRO-D-ARGININE is a valuable chemical tool for a wide range of research and practical applications in the fields of biochemistry and chemical biology.
Check Digit Verification of cas no
The CAS Registry Mumber 160347-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,3,4 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160347-94:
(8*1)+(7*6)+(6*0)+(5*3)+(4*4)+(3*7)+(2*9)+(1*4)=124
124 % 10 = 4
So 160347-94-4 is a valid CAS Registry Number.
160347-94-4Relevant articles and documents
Solid-phase total synthesis and structure proof of callipeltin B
Krishnamoorthy, Ravi,Vazquez-Serrano, Leslie D.,Turk, Jeffrey A.,Kowalski, Jennifer A.,Benson, Alan G.,Breaux, Nneka T.,Lipton, Mark A.
, p. 15392 - 15393 (2007/10/03)
The cytotoxic, cyclic heptadepsipeptide, natural product callipeltin B was synthesized on a solid-phase support in 15% overall yield. Comparison of the 1H NMR spectra of three synthetic isomers with those of callipeltin B confirmed the configurational reassignment of its threonine residues as d-allothreonine and the assignment of the configuration of its β-methoxytyrosine residue as (2R,3R). Copyright