3137-11-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of 1-(4-nitro-benzyl)-naphthalene.
Explanation
The core structure of 1-(4-nitro-benzyl)-naphthalene is a naphthalene molecule, which is a fused pair of benzene rings. A benzyl group (C6H5-CH2-) and a nitro group (-NO2) are attached to the naphthalene core.
Explanation
1-(4-nitro-benzyl)-naphthalene has distinct chemical and structural properties that make it useful in various applications, such as organic synthesis and chemical research.
Explanation
Due to its unique properties, 1-(4-nitro-benzyl)-naphthalene is used in the synthesis of various organic compounds, as well as in the production of industrial products and pharmaceuticals.
Explanation
1-(4-nitro-benzyl)-naphthalene is significant in various scientific and industrial applications due to its versatility and the diverse range of products and materials that can be derived from it.
Structure
Naphthalene core with a benzyl group and a nitro group attached
Chemical properties
Unique chemical and structural properties
Applications
Organic synthesis, chemical research, industrial products, and pharmaceuticals
Potential applications
Materials science and as a precursor for the synthesis of other organic compounds
Importance
Wide range of uses in scientific and industrial fields
Check Digit Verification of cas no
The CAS Registry Mumber 3137-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3137-11:
(6*3)+(5*1)+(4*3)+(3*7)+(2*1)+(1*1)=59
59 % 10 = 9
So 3137-11-9 is a valid CAS Registry Number.
3137-11-9Relevant articles and documents
Palladium and Nickel Catalyzed Suzuki Cross-Coupling with Alkyl Fluorides
Balaraman, Kaluvu,Wolf, Christian
supporting information, p. 8994 - 8999 (2021/11/20)
Suzuki cross-coupling of benzylic and unactivated aliphatic fluorides with aryl- and alkenylboronic acids has been achieved via mechanistically distinct Pd and Ni catalyzed pathways that outperform competing protodeboronation, β-hydride elimination, and h
A nonsymmetric pincer-catalyzed Suzuki-Miyaura arylation of benzyl halides and other nonactivated unusual coupling partners
Ines, Blanca,Moreno, Isabel,SanMartin, Raul,Dominguez, Esther
supporting information; experimental part, p. 8448 - 8451 (2009/04/11)
(Chemical Equation Presented) The catalytic activity of a PCN-type palladium pincer complex is evaluated in the construction of C(sp 2)-C(sp2) and C(sp2)-C(sp3) bonds by Suzuki-Miyaura cross-couplings employing nontypical substrates such as benzyl halides, α-haloenones, or alkylboronic acids as coupling partners. Most of the reported reactions are achieved in aqueous media, with all of the advantages implied.
