3150-34-3 Usage
Uses
Used in Organometallic Chemistry:
CpCp is used as a ligand for transition metals to improve the stability and reactivity of metal complexes. Its strong metal-carbon bonds and ability to activate and modify the reactivity of transition metal centers make it a vital component in this field.
Used in Catalysis:
CpCp is utilized in various catalytic processes, contributing to the efficiency and effectiveness of chemical reactions.
Used in Materials Science:
As a key component in the synthesis of a wide range of organometallic compounds, CpCp plays a significant role in the development of new materials with diverse applications in materials science.
Used in Organic Synthesis:
CpCp contributes to the synthesis of organometallic compounds that have applications in organic synthesis, aiding in the creation of complex organic molecules.
Used in Inorganic Synthesis:
Similarly, CpCp is employed in the synthesis of organometallic compounds that are utilized in inorganic synthesis, facilitating the production of inorganic materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 3150-34-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3150-34:
(6*3)+(5*1)+(4*5)+(3*0)+(2*3)+(1*4)=53
53 % 10 = 3
So 3150-34-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H26N6O15P2/c19-8-1-3-23(17(29)21-8)15-12(27)10(25)6(36-15)5-7(38-41(34,35)39-40(31,32)33)14-11(26)13(28)16(37-14)24-4-2-9(20)22-18(24)30/h1-4,6-7,10-16,25-28H,5H2,(H,34,35)(H2,19,21,29)(H2,20,22,30)(H2,31,32,33)/t6-,7?,10-,11+,12-,13-,14-,15-,16-/m1/s1
3150-34-3Relevant academic research and scientific papers
Phosphine-Mediated Bioconjugation of the 3′-End of RNA
Kitoun, Camélia,Fonvielle, Matthieu,Sakkas, Nicolas,Lefresne, Manon,Djago, Fabiola,Blancart Remaury, Quentin,Poinot, Pauline,Arthur, Michel,Etheve-Quelquejeu, Mélanie,Iannazzo, Laura
supporting information, p. 8034 - 8038 (2020/11/02)
Staudinger ligation is an attractive bio-orthogonal reaction that has been widely used to tag proteins, carbohydrates, and nucleic acids. Here, we explore the traceless variant of the Staudinger ligation for 3′-end modification of oligoribonucleotides. An azido-containing dinucleotide was used to study the ligation. Nine phosphines containing reactive groups, affinity purification tags, or photoswitch probes have been successfully obtained. The corresponding modified dinucleotides were synthesized and characterized by LC/MS. Mechanistic interpretations of the reaction are proposed, in particular, the unprecedented formation of an oxazaphospholane nucleotide derivative, which was favored by the vicinal position of 2′-N3 and 3′-OH functional groups on the terminal ribose has been observed. The post-functionalization of a 24-nt RNA with a photoactivable tag is also reported.
