6315-60-2 Usage
General Description
N,N-Di-(beta-carboethoxyethyl)methylamine is a chemical compound that belongs to the class of tertiary amines. It is a clear, colorless liquid with a faint ammonia-like odor and is commonly used as a reagent in organic synthesis processes, including the production of pharmaceuticals. N,N-DI-(BETA-CARBOETHOXYETHYL)METHYLAMINE is also used in the manufacturing of dyes, surfactants, and corrosion inhibitors. In addition, it can act as a catalyst in reactions involving the formation of carbon-carbon and carbon-nitrogen bonds. N,N-Di-(beta-carboethoxyethyl)methylamine is considered to be moderately toxic and requires careful handling and storage to prevent any potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 6315-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6315-60:
(6*6)+(5*3)+(4*1)+(3*5)+(2*6)+(1*0)=82
82 % 10 = 2
So 6315-60-2 is a valid CAS Registry Number.
6315-60-2Relevant articles and documents
DIMER COMPOUNDS, AND USE IN BINDING TOXIC REPEATS OF RNA
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Paragraph 0260; 0261, (2020/07/16)
Provided herein are compounds and methods for modulating abnormal repeat expansions of gene sequences. More particularly, provided are dimeric inhibitors of RNA and the uses of such inhibitors in regulating nucleotide repeat expansions, e.g., to treat Myotonic Dystrophy Type 1 (DM1), Myotonic Dystrophy Type 2 (DM2), Fuchs dystrophy, Huntington Disease, Amyotrophic Lateral Sclerosis, or Frontotemporal Dementia.
A new stepwise synthesis of a family of propylamines derived from diatom silaffins and their activity in silicification
Annenkov, Vadim V.,Patwardhan, Siddharth V.,Belton, David,Danilovtseva, Elena N.,Perry, Carole C.
, p. 1521 - 1523 (2008/02/11)
A new method for the stepwise synthesis of propylamines containing fragments of N-methyl propylamine as found in diatom bioextracts is presented and their activity in silicic acid condensation is described. The Royal Society of Chemistry 2006.
