832-97-3 Usage
Description
DL-INDOLE-3-LACTIC ACID is a chiral organic compound that serves as an important intermediate in the synthesis of various pharmaceuticals and biologically active molecules. It is characterized by its unique structure, which includes an indole ring and a lactate group, making it a versatile building block in organic chemistry.
Used in Pharmaceutical Industry:
DL-INDOLE-3-LACTIC ACID is used as a reactant for the preparation of antibacterial agents, contributing to the development of new drugs to combat bacterial infections. Its unique structure allows for the creation of molecules with potent antibacterial properties, addressing the growing need for effective treatments against drug-resistant bacteria.
Used in Food Industry:
DL-INDOLE-3-LACTIC ACID is used as a reactant for the preparation of dietary sweeteners, offering a potential alternative to traditional sweeteners. Its ability to be synthesized into sweet-tasting compounds makes it a valuable component in the development of new, healthier sweeteners for the food and beverage industry.
Check Digit Verification of cas no
The CAS Registry Mumber 832-97-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 832-97:
(5*8)+(4*3)+(3*2)+(2*9)+(1*7)=83
83 % 10 = 3
So 832-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-11(15,10(13)14)8-6-12-9-5-3-2-4-7(8)9/h2-6,12,15H,1H3,(H,13,14)
832-97-3Relevant articles and documents
Biocontrolled formal inversion or retention of L -α-amino acids to enantiopure (R)- or (S)-hydroxyacids
Busto, Eduardo,Grischek, Barbara,Kroutil, Wolfgang,Richter, Nina
supporting information, p. 11225 - 11228,4 (2015/01/07)
Natural L-α-amino acids and L-norleucine were transformed to the corresponding α-hydroxy acids by formal biocatalytic inversion or retention of absolute configuration. The one-pot transformation was achieved by a concurrent oxidation reduction cascade in aqueous media. A representative panel of enantiopure (R)- and (S)-2-hydroxy acids possessing aliphatic, aromatic and heteroaromatic moieties were isolated in high yield (67-85 %) and enantiopure form (>99 % ee) without requiring chromatographic purification.
Preparation of 3-(3-indolyl)lactic acids. A new synthesis of rac-blepharismone, the low molecular conjugation gamone of Blepharisma japonicum
Entzeroth,Kunczik,Jaenicke
, p. 226 - 230 (2007/10/02)
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