121570-10-3 Usage
General Description
(3S)-3-Methyl-D-aspartic acid, also known as 3-Methyl-D-aspartic acid, is a unique and specific agonist for the N-methyl-D-aspartate (NMDA) receptor. This chemical is a derivative of the neurotransmitter glutamate and is naturally occurring in the brain. It has been shown to play a role in various physiological processes, including modulating synaptic plasticity, learning, and memory. Additionally, it has been found to have potential neuroprotective effects and may be involved in the regulation of hormone levels. Studies have also suggested that (3S)-3-Methyl-D-aspartic acid may have potential therapeutic applications in the treatment of neurological disorders and cognitive impairments. Overall, this chemical is a fascinating compound with important implications for neuroscience and potential clinical significance.
Check Digit Verification of cas no
The CAS Registry Mumber 121570-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121570-10:
(8*1)+(7*2)+(6*1)+(5*5)+(4*7)+(3*0)+(2*1)+(1*0)=83
83 % 10 = 3
So 121570-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO4/c1-2(4(7)8)3(6)5(9)10/h2-3H,6H2,1H3,(H,7,8)(H,9,10)/t2-,3+/m1/s1
121570-10-3Relevant articles and documents
Indium-mediated allylation and Reformatsky reaction on glyoxylic oximes under ultrasound irradiation
Soengas, Raquel G.,Estévez, Amalia M.
experimental part, p. 916 - 920 (2012/06/04)
A novel and more convenient method for the indium-promoted allylation of glyoxylic oximes based on the use of ultrasonic waves is reported. A similar procedure was used to develop the first example reported in the literature of an indium-mediated Reformatsky reaction on oxime ethers.
SYNTHESIS AND ABSOLUTE STEREOCHEMISTRY OF SERRICORNIN
Mori, Kenji,Nomi, Hiroko,Chuman, Tatsuji,Kohno, Masahiro,Kato, Kunio,Noguchi, Masao
, p. 3705 - 3712 (2007/10/02)
The absolute stereochemistry of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone) was established as 4S, 6S, 7S by synthesizing both (4S, 6S, 7S)-isomer and its antipode.Only the natural enantiomer was bioactive.by