32350-46-2 Usage
Description
(2Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid, also known as N-tert-Butylglycine, is a chiral alpha-amino acid derivative with the molecular formula C10H17NO3. It features both a carboxylic acid group and an amino group, and is characterized by the (2Z) geometry of its double bond. This chemical compound serves as a versatile building block in the pharmaceutical industry for the synthesis of a variety of compounds and holds potential for the development of new drugs and biologically active molecules.
Uses
Used in Pharmaceutical Industry:
(2Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid is used as a building block for the synthesis of various compounds, contributing to the development of new drugs and biologically active molecules. Its unique structure and chirality make it a valuable component in the creation of pharmaceuticals with specific therapeutic properties.
Used in Research and Development:
(2Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid is also used in research and development for its potential biological activity. The exploration of its properties and interactions with biological systems can lead to the discovery of new applications and therapeutic uses, further expanding its utility in the scientific community.
Used in Drug Synthesis:
(2Z)-4-(tert-butylamino)-4-oxobut-2-enoic acid is utilized as a precursor in the synthesis of other biologically active molecules. Its presence in the molecular structure can influence the pharmacological properties of the final product, making it an important component in the development of innovative drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 32350-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32350-46:
(7*3)+(6*2)+(5*3)+(4*5)+(3*0)+(2*4)+(1*6)=82
82 % 10 = 2
So 32350-46-2 is a valid CAS Registry Number.
32350-46-2Relevant articles and documents
Terification of maleamic acids without double bond isomerization
Sanchez, Albert,Pedroso, Enrique,Grandas, Anna
experimental part, p. 2600 - 2606 (2010/09/07)
Activation of the carboxylic acid group of a maleamic acid by treatment with an arenesulfonyl chloride followed by addition of an alcohol affords a fumaramate or a maleamate, depending on the reaction conditions. The E isomer is obtained when the acid is treated with nearly equimolar amounts of 2,4,6-triisopropylbenzenesulfonyl chloride and an alcohol in pyridine. Replacement of pyridine by 2-picoline and use of a larger excess of activating agent (mesitylenesulfonyl chloride) and alcohol affords the Z isomer. In both cases, high diastereomeric excesses and yields are achieved.
Secondary aspartic acid amide esters
-
, (2008/06/13)
New secondary amines are described which are prepared from inexpensive, commercially available raw materials, are stable at room temperature, and are reactive toward electrophiles. The secondary amines are prepared by the addition of one or more primary amines with one or more male (amide/ester) and fumar (amide/ester) Michael receptors. The above amines can be used as coreactants with aliphatic polyisocyanates for polyurea coatings. The novel secondary amines are also described as particularly useful as part of a two-part liquid pavement marking composition for pavement markings.
[2+2]-cycloaddition of 'maleic isoimides' with ketenes and reactions of spiro-β-lactams to muconic and tetramic acids
Capraro,Winkler,Martin
, p. 362 - 378 (2007/10/02)
-