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121570-10-3

(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.

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  • 121570-10-3 Structure

  • Basic information

    1. Product Name: (3S)-3-Methyl-D-aspartic acid
    2. Synonyms: (2S,3R)-2-Amino-3-methylsuccinic acid;(3S)-3-Methyl-D-aspartic acid
    3. CAS NO:121570-10-3
    4. Molecular Formula: C5H9NO4
    5. Molecular Weight: 147.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121570-10-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 259 ºC
    3. Flash Point: 111 ºC
    4. Appearance: /
    5. Density: 1.404
    6. Vapor Pressure: 0.004mmHg at 25°C
    7. Refractive Index: 1.519
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3S)-3-Methyl-D-aspartic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3S)-3-Methyl-D-aspartic acid(121570-10-3)
    12. EPA Substance Registry System: (3S)-3-Methyl-D-aspartic acid(121570-10-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 121570-10-3(Hazardous Substances Data)

121570-10-3 Usage

Uses

Used in Pharmaceutical Industry:
(3S)-3-Methyl-D-aspartic acid is used as a therapeutic agent for the treatment of neurological disorders and cognitive impairments due to its potential neuroprotective effects and involvement in the regulation of hormone levels.
Used in Neuroscience Research:
(3S)-3-Methyl-D-aspartic acid is used as a research tool for studying the role of NMDA receptors in synaptic plasticity, learning, and memory, as well as its potential involvement in the regulation of hormone levels.

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

121570-10-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name D,L-threo-β-methylaspartic acid

1.2 Other means of identification

Product number -
Other names (2S,3R)-2-AMINO-3-METHYLSUCCINIC ACID

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:121570-10-3 SDS

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.

Organocatalytic synthesis of β-alkylaspartates via β-lactone ring opening

Armstrong, Alan,Geldart, Stephen P.,Jenner, Chloe R.,Scutt, James N.

, p. 8091 - 8094 (2008/02/13)

(Chemical Equation Presented) Cinchona alkaloid-catalyzed reaction of ethyl glyoxylate with substituted ketenes, formed in situ, gives disubstituted β-lactones in moderate yield and high enantiomeric excess. Subsequent azide ring opening, reduction, and e

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

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