62978-52-3 Usage
General Description
Methyl 4-[bis(2-chloroethyl)amino]phenylalaninate is a chemical compound that is commonly known as sarin, a potent nerve agent and chemical weapon. It is a toxic and highly dangerous organophosphorus compound that acts by inhibiting the enzyme acetylcholinesterase, leading to the accumulation of the neurotransmitter acetylcholine in the nervous system. Exposure to sarin can cause a range of symptoms, including muscle twitching, respiratory distress, and ultimately paralysis and death. It is classified as a weapon of mass destruction and is strictly regulated under international treaties. Its production, stockpiling, and use are prohibited, and efforts are ongoing to eliminate existing stockpiles and prevent its proliferation.
Check Digit Verification of cas no
The CAS Registry Mumber 62978-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,7 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62978-52:
(7*6)+(6*2)+(5*9)+(4*7)+(3*8)+(2*5)+(1*2)=163
163 % 10 = 3
So 62978-52-3 is a valid CAS Registry Number.
62978-52-3Relevant articles and documents
PROCESS FOR THE PREPARATION OF MELPHALAN HYDROCHLORIDE
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Page/Page column 2, (2012/05/20)
The present invention provides a simple and efficient method for synthesis of 4-[bis (2-chloroethyl)-amino]-L-phenylalanine hydrochloride. The process involves the treatment of 4-[bis(2-chloroethyl)-amino]-L-phenylalanine free base with hydrochloric acid in water followed by isolation of 4-[bis(2-chloroethyl)-amino]-phenylalanine hydrochloride of desired purity.
Alkylating Angiotensin II Analogues: Synthesis, Analysis, and Biological Activity of Angiotensin II Analogues Containing the Nitrogen Mustard Melphalan in Position 8
Hsieh, Kun-hwa,Marshall, Garland R.
, p. 1304 - 1310 (2007/10/02)
Melphalan derivatives suitable for peptide synthesis, i.e., Boc-Mel and Mel-OBzl*HCl, have been prepared, and the integrity of their nitrogen mustard alkylating groups was examined by NMR, Volhard chlorine analysis, and colorimetric assay with 4-(p-nitrob