2799-58-8 Usage
General Description
BIS(2-CHLOROETHYL) METHYLPHOSPHONATE, also known as BCM, is a toxic chemical compound that is primarily used as a chemical warfare agent. It is a potent alkylating agent that can cause a range of harmful effects on the body, including respiratory and neurological toxicity, skin and eye irritation, and damage to the gastrointestinal system. BCM is classified as a Schedule 1 chemical under the Chemical Weapons Convention, and its production and stockpiling are strictly regulated. Due to its extreme toxicity and potential for use as a weapon of mass destruction, BCM is considered a highly dangerous substance and is subject to strict controls and international treaties.
Check Digit Verification of cas no
The CAS Registry Mumber 2799-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2799-58:
(6*2)+(5*7)+(4*9)+(3*9)+(2*5)+(1*8)=128
128 % 10 = 8
So 2799-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H11Cl2O3P/c1-11(8,9-4-2-6)10-5-3-7/h2-5H2,1H3
2799-58-8Relevant articles and documents
GC-MS Study of Mono- and Bishaloethylphosphonates Related to Schedule 2.B.04 of the Chemical Weapons Convention: The Discovery of a New Intramolecular Halogen Transfer
Picazas-Márquez, Nerea,Sierra, María,Nova, Clara,Moreno, Juan Manuel,Aboitiz, Nuria,de Rivas, Gema,Sierra, Miguel A.,Martínez-álvarez, Roberto,Gómez-Caballero, Esther
, p. 1510 - 1519 (2016/08/13)
A new class of compounds, mono- and bis-haloethylphosphonates (HAPs and bisHAPs, respectively), listed in Schedule 2.B.04 of the Chemical Weapons Convention (CWC), has been synthesized and studied by GC-MS with two aims. First, to improve the identification of this type of chemicals by the Organization for the Prohibition of Chemical Weapons, (OPCW). Second, to study the synergistic effect of halogen and silicon atoms in molecules undergoing mass spectrometry. Fragmentation patterns of trimethylsilyl derivatives of HAPs were found to depend on the nature of the halogen atom; this was in agreement with DFT-calculations. The data suggest that a novel intramolecular halogen transfer takes place during the fragmentation process. [Figure not available: see fulltext.]
