19036-43-2 Usage
Description
3-AMINO-2,2-DIMETHYL-PROPANOIC ACID is a chemical compound characterized by its molecular formula C6H13NO2. It is a derivative of propanoic acid, featuring both a carboxylic acid group and an amino group. This white crystalline solid has a molecular weight of 131.17 g/mol and is known for its versatility in the pharmaceutical and chemical industries.
Uses
Used in Pharmaceutical Industry:
3-AMINO-2,2-DIMETHYL-PROPANOIC ACID is used as a building block in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can have therapeutic effects.
Used in Chemical Industry:
3-AMINO-2,2-DIMETHYL-PROPANOIC ACID is used as a reagent in organic synthesis, facilitating various chemical reactions that are essential in the creation of new compounds.
Used in Research and Development:
3-AMINO-2,2-DIMETHYL-PROPANOIC ACID is utilized in the development of new chemical compounds, serving as a key intermediate that can lead to innovative products and materials.
Used as an Intermediate in Chemical Production:
3-AMINO-2,2-DIMETHYL-PROPANOIC ACID is used in the production of various other chemicals, playing a crucial role as an intermediate that helps in the synthesis of a wide range of end products.
Check Digit Verification of cas no
The CAS Registry Mumber 19036-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,3 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19036-43:
(7*1)+(6*9)+(5*0)+(4*3)+(3*6)+(2*4)+(1*3)=102
102 % 10 = 2
So 19036-43-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-5(2,3-6)4(7)8/h3,6H2,1-2H3,(H,7,8)
19036-43-2Relevant articles and documents
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Johnson
, p. 126 (1968)
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Palladium(0)/PAr3-catalyzed intermolecular amination of C(sp3)-H bonds: Synthesis of β-amino acids
He, Jian,Shigenari, Toshihiko,Yu, Jin-Quan
, p. 6545 - 6549 (2015/06/08)
An intermolecular C(sp3)-H amination using a Pd0/PAr3 catalyst was developed. The reaction begins with oxidative addition of R2N-OBz to a Pd0/PAr3 catalyst and subsequent cleavage of a C(sp3)-H bond by the generated Pd-NR2 intermediate. The catalytic cycle proceeds without the need for external oxidants in a similar manner to the extensively studied palladium(0)-catalyzed C-H arylation reactions. The electron-deficient triarylphosphine ligand is crucial for this C(sp3)-H amination reaction to occur.
NOVEL COMPOUND HAVING ABILITY TO INHIBIT 11B-HSD1 ENZYME OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD FOR PRODUCING SAME, AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT
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, (2015/05/06)
The present invention relates to a novel compound or a pharmaceutically acceptable salt thereof inhibiting 11β-HSD1 enzyme activity, a preparation method of the same, and a pharmaceutical composition comprising the same as an active ingredient. Since the compound of the present invention selectively inhibits the activity of 11β-HSD1 (11β-Hydroxysteroid dehydrogenase type 1), the compound of the invention can be effectively used as a therapeutic agent for the treatment of diseases caused by the over-activation of 11β-HSD1 such as non-insulin dependent type II diabetes, insulin resistance, obesity, lipid disorder, metabolic syndrome, and other diseases or condition mediated by the excessive activity of glucocorticoid.