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28954-12-3

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28954-12-3 Usage

Description

L(+)-allo-Threonine, also known as allothreonine, is a white to off-white crystalline powder with unique chemical properties. It is an isomer of the naturally occurring L-threonine, which differs in the spatial arrangement of its atoms. This synthetic amino acid is not commonly found in nature but has significant applications in various industries due to its distinct properties.

Uses

Used in Pharmaceutical Industry:
L(+)-allo-Threonine is used as a reactant for the synthesis of specific antibiotics, such as globomycin and its congener, SF-1902 A5. These antibiotics are employed to treat various bacterial infections, highlighting the importance of L(+)-allo-Threonine in the development of pharmaceutical compounds.
In the synthesis of these antibiotics, L(+)-allo-Threonine serves as a crucial building block, contributing to the overall structure and function of the final product. Its unique properties allow for the creation of antibiotics with specific modes of action, targeting and eliminating harmful bacteria effectively.
Overall, L(+)-allo-Threonine is a valuable compound in the pharmaceutical industry, playing a vital role in the development and synthesis of antibiotics that help combat bacterial infections and improve public health.

Check Digit Verification of cas no

The CAS Registry Mumber 28954-12-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,5 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28954-12:
(7*2)+(6*8)+(5*9)+(4*5)+(3*4)+(2*1)+(1*2)=143
143 % 10 = 3
So 28954-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m0/s1

28954-12-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (A1519)  L-Allothreonine  >99.0%(HPLC)

  • 28954-12-3

  • 100mg

  • 1,130.00CNY

  • Detail
  • TCI America

  • (A1519)  L-Allothreonine  >99.0%(HPLC)

  • 28954-12-3

  • 1g

  • 3,690.00CNY

  • Detail
  • Alfa Aesar

  • (H27301)  L-allo-Threonine, 99%   

  • 28954-12-3

  • 250mg

  • 1431.0CNY

  • Detail
  • Alfa Aesar

  • (H27301)  L-allo-Threonine, 99%   

  • 28954-12-3

  • 1g

  • 3822.0CNY

  • Detail
  • Aldrich

  • (210269)  L-allo-Threonine  99%

  • 28954-12-3

  • 210269-250MG

  • 3,061.89CNY

  • Detail

28954-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name L-allothreonine

1.2 Other means of identification

Product number -
Other names (2S,3S)-2-amino-3-hydroxybutanoic 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:28954-12-3 SDS

28954-12-3Relevant articles and documents

Noncovalently Functionalized Commodity Polymers as Tailor-Made Additives for Stereoselective Crystallization

Wan, Xinhua,Wang, Zhaoxu,Ye, Xichong,Zhang, Jie

supporting information, p. 20243 - 20248 (2021/08/09)

Stereoselective inhibition of the nucleation and crystal growth of one enantiomer aided by “tailor-made” polymeric additives is an efficient method to obtain enantiopure compounds. However, the conventional preparation of polymeric additives from chiral monomers are laborious and limited in structures, which impedes their rapid optimization and applicability. Herein, we report a “plug-and-play” strategy to facilitate synthesis by using commercially available achiral polymers as the platform to attach various chiral small molecules as the recognition side-chains through non-covalent interactions. A library of supramolecular polymers made up of two vinyl polymers and six small molecules were applied with seeds in the selective crystallization of seven racemates in different solvents. They showed good to excellent stereoselectivity in yielding crystals with high enantiomeric purities in conglomerates and racemic compound forming systems. This convenient, low-cost modular synthesis strategy of polymeric additives will allow for high-efficient, economical resolution of various racemates on different scales.

Colony-wise Analysis of a Theonella swinhoei Marine Sponge with a Yellow Interior Permitted the Isolation of Theonellamide i

Fukuhara, Kazuya,Takada, Kentaro,Watanabe, Ryuichi,Suzuki, Toshiyuki,Okada, Shigeru,Matsunaga, Shigeki

, p. 2595 - 2599 (2018/12/13)

There are several examples of marine organisms whose metabolic profiles differ among conspecifics inhabiting the same region. We have analyzed the metabolic profile of each colony of a Theonella swinhoei marine sponge with a yellow interior and noticed the patchy distribution of one metabolite. This compound was isolated and its structure was studied by a combination of spectrometric analyses and chemical degradation, showing it to be a congener in the theonellamide class of bicyclic peptides. Theonellamides had previously been isolated by us only from T. swinhoei with a white interior and not from those with a yellow interior.

A α - amino acid compound synthesis and purification method

-

Paragraph 0069; 0070, (2018/05/16)

The invention relates to a synthesis and purification method for an alpha-amino acid compound. The synthesis and purification method is characterized by comprising the following steps: (1) adding substituted alpha-amino nitrile or a substituted hydantoin-based compound into alkali M(OH)x or metal oxide MxO, adding water or an alcohol and water mixed solvent, and heating for reaction to obtain alpha-amino acid salt; (2) adding ammonium carbonate or ammonium bicarbonate or introducing carbon dioxide into the solution in the step (1), separating to obtain filter liquor and precipitates MxHyCO3, performing reduced pressure concentration on the filter liquor, and recrystallizing in an alcohol solvent to obtain the alpha-amino acid compound (I). The synthesis and purification method for the alpha-amino acid compound is simple, the yield and purity of the obtained alpha-amino acid compound are high; furthermore, recycling utilization and cleaning production of materials can be realized; the synthesis and purification method is especially suitable for synthesis of the alpha-amino acid compound with high water solubility.

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