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19872-93-6

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19872-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19872-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,7 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19872-93:
(7*1)+(6*9)+(5*8)+(4*7)+(3*2)+(2*9)+(1*3)=156
156 % 10 = 6
So 19872-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO5/c1-14-6-4-7(9(12)15-2)11-8(5-6)10(13)16-3/h4-5H,1-3H3

19872-93-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 4-methoxypyridine-2,6-dicarboxylate

1.2 Other means of identification

Product number -
Other names dimethyl 4-methoxy-2,6-pyridinedicarboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19872-93-6 SDS

19872-93-6Relevant articles and documents

Electronic: Versus steric effects of pyridinophane ligands on Pd(III) complexes

Tang, Fengzhi,Park, Sungho V.,Rath, Nigam P.,Mirica, Liviu M.

, p. 1151 - 1158 (2018)

Several new PdII and PdIII complexes supported by electronically and sterically tuned tetradentate pyridinophane ligands MeN4OMe, MeN4, and tBuN4 were isolated and fully characterized (MeN4OMe: N,N′-dimethyl-2,11-diaza[3,3](2,6)-para-methoxypyridinophane; MeN4: N,N′-dimethyl-2,11-diaza[3,3](2,6)pyridinophane; tBuN4: N,N′-di-tert-butyl-2,11-diaza[3,3](2,6)pyridinophane). Cyclic voltammetry studies, UV-vis and EPR spectroscopy, and X-ray crystallography were employed to reveal that the steric properties of the N-substituents of the RN4 ligands have a pronounced effect on the electronic properties of the corresponding PdIII complexes, while the electronic tuning of the ligand pyridyl groups has a surprisingly minimal effect. An explanation for these observations was provided by DFT and TD-DFT calculations which suggest that the electronic properties of the PdIII complexes are mainly dictated by their frontier molecular orbitals that have major atomic contributions from the Pd center (mainly the Pd dz2 atomic orbital) and the axial N atom donors.

Sulfur transfer reactions of a zinc tetrasulfanido complex

Ballesteros Ii, Moises,Tsui, Emily Y.

, p. 16305 - 16311 (2020)

A zinc tetrasulfanido complex supported by a bis(carboxamide)pyridine ligand framework has been synthesized by the insertion of elemental sulfur into the zinc-S(thiolate) bond of a zinc dithiolate complex ([LZn]2-). This paper reports on sulfur transfer reactions of this polysulfanido complex ([1]2-) and compares this behavior to known reactions of metal polysulfido complexes. Complex [1]2- was demonstrated to be in exchange with [LZn]2- and free elemental sulfur in solution. Although triphenylphosphine abstracts sulfur from [1]2- to form [LZn]2-, complex [LZn]2- can abstract sulfur from the zinc polysulfido complex (TMEDA)ZnS6 (TMEDA = N,N,N′,N′-tetramethylethylenediamine). The tetrasulfanido complex [1]2- can also transfer sulfur to dimethyl acetylenedicarboxylate to form a zinc dithiolene complex. These studies demonstrate that the zinc complex with a tetrasulfanido moiety can undergo similar reactions as metal complexes with purely inorganic polysulfido groups, although the final metal-containing products are different.

COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PAIN

-

Page/Page column 70; 72, (2019/08/26)

The invention relates to compounds, pyridine derivatives, and pharmaceutical 10 compositions containing same for use in the treatment of pain. It also relates to specific compounds, compositions comprising the same and uses thereof, in particular in the treatment of pain.

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