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2,3-Diaminobutyric acid (DABA) is an organic compound that is typically white and non-flammable, classified as a rare amino acid not incorporated into proteins. With a molecular weight of 118.14 g/mol and a chemical formula of C4H10N2O2, it serves as a fundamental building block in scientific research and pharmaceutical development.

2643-66-5

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2643-66-5 Usage

Uses

Used in Scientific Research:
2,3-Diaminobutyric acid is used as a starting material for the preparation of various pharmaceutical agents, contributing to the advancement of medicinal chemistry and drug discovery.
Used in Pharmaceutical Development:
2,3-Diaminobutyric acid is used as a precursor in the synthesis of bioactive compounds, facilitating the creation of new therapeutic agents with potential applications in medicine.
Used in Bacterial and Plant Studies:
2,3-Diaminobutyric acid is used in the study of certain bacteria and plants where it has been found, aiding in understanding its biological role and potential interactions within these organisms.
Caution:
Despite its applications, 2,3-Diaminobutyric acid can be toxic if improperly handled or ingested, necessitating careful and responsible use in research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 2643-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,4 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2643-66:
(6*2)+(5*6)+(4*4)+(3*3)+(2*6)+(1*6)=85
85 % 10 = 5
So 2643-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2O2/c1-2(5)3(6)4(7)8/h2-3H,5-6H2,1H3,(H,7,8)

2643-66-5SDS

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 2,3-diaminobutanoic acid

1.2 Other means of identification

Product number -
Other names 2,3-Diamino-buttersaeure

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:2643-66-5 SDS

2643-66-5Downstream Products

2643-66-5Relevant academic research and scientific papers

Totopotensamides, polyketide-cyclic peptide hybrids from a mollusk-associated bacterium Streptomyces sp.

Lin, Zhenjian,Flores, Malem,Forteza, Imelda,Henriksen, Niel M.,Concepcion, Gisela P.,Rosenberg, Gary,Haygood, Margo G.,Olivera, Baldomero M.,Light, Alan R.,Cheatham, Thomas E.,Schmidt, Eric W.

experimental part, p. 644 - 649 (2012/06/29)

Two new compounds, the peptide-polyketide glycoside totopotensamide A (1) and its aglycone totopotensamide B (2), were isolated from a Streptomyces sp. cultivated from the gastropod mollusk Lienardia totopotens collected in the Philippines. The compounds contain a previously undescribed polyketide component, a novel 2,3-diaminobutyric acid-containing macrolactam, and a new amino acid, 4-chloro-5,7-dihydroxy-6-methylphenylglycine. The application of Marfey's method to phenylglycine derivatives was explored using quantum mechanical calculations and NMR.

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