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2812-31-9

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2812-31-9 Usage

Description

N(alpha),N(alpha)-Dimethylalanine, also known as a methyl-L-alanine, is an amino acid derivative where both the amino hydrogens of L-alanine are replaced by methyl groups. This modification results in a unique structure and properties that can be utilized in various applications across different industries.

Uses

Used in Pharmaceutical Industry:
N(alpha),N(alpha)-Dimethylalanine is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of novel drugs with potential therapeutic applications, such as targeting specific receptors or enzymes in the body.
Used in Chemical Synthesis:
In the field of chemical synthesis, N(alpha),N(alpha)-Dimethylalanine serves as an important intermediate for the production of complex organic molecules. Its distinct properties enable the creation of new compounds with specific functionalities, which can be applied in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
N(alpha),N(alpha)-Dimethylalanine is utilized as a research tool in the study of protein structure, function, and interactions. Its unique properties allow scientists to investigate the effects of amino acid modifications on protein stability, folding, and binding affinity. This knowledge can be applied to the design of new proteins and peptides with improved or novel functions.
Used in Analytical Chemistry:
N(alpha),N(alpha)-Dimethylalanine can be employed as a reference compound or internal standard in various analytical techniques, such as chromatography and mass spectrometry. Its distinct properties make it suitable for comparing and quantifying other compounds in complex mixtures, contributing to the advancement of analytical methods and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 2812-31-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2812-31:
(6*2)+(5*8)+(4*1)+(3*2)+(2*3)+(1*1)=69
69 % 10 = 9
So 2812-31-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-4(5(7)8)6(2)3/h4H,1-3H3,(H,7,8)

2812-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-L-alanine

1.2 Other means of identification

Product number -
Other names N,N-Dimethyl-DL-Alanine

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:2812-31-9 SDS

2812-31-9Upstream product

2812-31-9Relevant articles and documents

Jubanines F-J, cyclopeptide alkaloids from the roots of Ziziphus jujuba

Kang, Kyo Bin,Ming, Gao,Kim, Geum Jin,Ha, Thi-Kim-Quy,Choi, Hyukjae,Oh, Won Keun,Sung, Sang Hyun

, p. 90 - 95 (2016/03/04)

Five Ib-type cyclopeptide alkaloids, jubanines F-J (1-5), and three known compounds, nummularine B (6), daechuine-S3 (7), and mucronine K (8) were isolated from the roots of Ziziphus jujuba. Their structures were fully characterized by spectroscopic analyses in combination with chemical derivatization. Compounds 1-3, and 6 were evaluated for their antiviral activity against the porcine epidemic diarrhea virus (PEDV). Compounds 2, 3, and 6 showed potent inhibitory effects on PEDV replication.

Cyclopeptide alkaloids of Zizyphus xylopyra

Rai, Nisha,Singh, Sarita,Singh,Pandey

experimental part, p. 336 - 337 (2009/06/25)

14-Membered cyclopeptide alkaloids, franganine, frangufoline, amphibine-D and mauritine-A has been isolated from the whole plant of Zizyphus xylopyra and their structures established by spectral evidences. This is the first report of these alkaloids from Z. xylopyra.

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