14328-54-2 Usage
Description
2-AMINO-3-ETHYL-PENTANOIC ACID, also known as β,β-Diethylalanine (CAS# 14328-54-2), is an organic compound with the chemical structure featuring an amino group and an ethyl group attached to a pentanoic acid backbone. It is a white solid and is primarily used in organic synthesis due to its unique chemical properties.
Uses
Used in Organic Synthesis:
2-AMINO-3-ETHYL-PENTANOIC ACID is used as a building block for the synthesis of various complex organic molecules. Its unique structure allows it to be a versatile component in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-AMINO-3-ETHYL-PENTANOIC ACID is used as an intermediate for the development of new drugs. Its specific functional groups can be exploited to create novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
2-AMINO-3-ETHYL-PENTANOIC ACID is also utilized as a starting material in the agrochemical industry for the synthesis of bioactive compounds, such as pesticides and herbicides, that can help improve crop yield and protect plants from pests.
Used in Specialty Chemicals:
The compound is employed as a key component in the production of specialty chemicals, which find applications in various industries, including cosmetics, coatings, and materials science. Its unique properties enable the development of innovative products with specific functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 14328-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,2 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14328-54:
(7*1)+(6*4)+(5*3)+(4*2)+(3*8)+(2*5)+(1*4)=92
92 % 10 = 2
So 14328-54-2 is a valid CAS Registry Number.
14328-54-2Relevant articles and documents
Process for the synthesis of chirally pure beta-amino-alcohols
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, (2008/06/13)
A process is provided for preparing chirally pure S-enantiomers of α-amino acids comprising the steps of: a) preparing an organometallic reagent from an alkyl halide of the formula (R)2CH(CH2)nCH2X; b) adding th
Synthesis of L α amino acids structurally related to isoleucine
Praetorius,Flossdorf,Kula
, p. 3079 - 3090 (2007/10/05)
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The synthesis of tenuazonic and congeneric tetramie acids.
Harris,Fisher,Folkers
, p. 478 - 482 (2007/10/05)
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