2013-91-4 Usage
Uses
Used in Organic Synthesis:
[(dimethylamino)methylene]dimethylammonium methyl sulphate is used as a phase-transfer catalyst for enhancing the efficiency of organic synthesis reactions. It facilitates the transfer of reactants between different phases, enabling smoother and more effective reactions.
Used in Polymer Industry:
In the polymer industry, [(dimethylamino)methylene]dimethylammonium methyl sulphate serves as a stabilizer for certain types of polymers. Its presence helps maintain the stability and integrity of the polymers during processing and use.
Used in Chemical Production:
[(dimethylamino)methylene]dimethylammonium methyl sulphate is also utilized as a reactant in the production of other chemicals. Its unique structure allows it to participate in various chemical reactions, contributing to the synthesis of a range of compounds.
Safety Precautions:
It is crucial to handle [(dimethylamino)methylene]dimethylammonium methyl sulphate with care, as it is a potential irritant. Inhalation of [(dimethylamino)methylene]dimethylammonium methyl sulphate may lead to respiratory issues, so proper safety measures should be taken to minimize exposure and ensure the well-being of those working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 2013-91-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2013-91:
(6*2)+(5*0)+(4*1)+(3*3)+(2*9)+(1*1)=44
44 % 10 = 4
So 2013-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H13N2.CH4O4S/c1-6(2)5-7(3)4;1-5-6(2,3)4/h5H,1-4H3;1H3,(H,2,3,4)/q+1;/p-1
2013-91-4Relevant academic research and scientific papers
NEW PROCESSES
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Page/Page column 135, (2009/08/16)
The invention relates to a new process for producing NEP inhibitors or prodrugs thereof, in particular NEP inhibitors comprising a γ-amino-δ-biphenyl-α-methylalkanoic acid, or acid ester, backbone. In detail, the new processes, according to the present invention, are ultimately related to the synthesis of intermediates to prepare the above NEP inhibitors, namely compounds according to formula (1), or salt thereof, wherein R1 and R2 are, independently of each other, hydrogen or a nitrogen protecting group, and R3 is a carboxyl group or an ester group, preferably carboxyl group or alkyl ester.
Reaction of Singlet Oxygen with Enamino Carbonyl Systems. A General Method for the Synthesis of α-Keto Derivatives of Lactones, Esters, Amides, Lactams, and Ketones
Wasserman, Harry H.,Ives, Jeffrey L.
, p. 3573 - 3580 (2007/10/02)
A general method for the introduction of a ketone α to the carbonyl group of a ketone, lactone. ester, substituted amide, or lactam has been developed involving the formation and dye-sensitized photooxygenation of enamino carbonyl intermediates.
