439116-13-9 Usage
Uses
Used in Chemical Research and Pharmaceutical Development:
(2-AMINOMETHYL-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is utilized as a reagent in chemical research and pharmaceutical development, contributing to the advancement of new chemical entities and therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-AMINOMETHYL-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER is employed for its potential biological and pharmacological activities, which may lead to the discovery of new drugs and treatments.
Used in Organic Synthesis:
Due to its unique chemical structure and reactivity, (2-AMINOMETHYL-BENZYL)-CARBAMIC ACID TERT-BUTYL ESTER serves as a building block in the synthesis of a variety of organic compounds, expanding the scope of chemical and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 439116-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,1,1 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 439116-13:
(8*4)+(7*3)+(6*9)+(5*1)+(4*1)+(3*6)+(2*1)+(1*3)=139
139 % 10 = 9
So 439116-13-9 is a valid CAS Registry Number.
439116-13-9Relevant academic research and scientific papers
DIAMINO-ALKYLAMINO-LINKED ARYLSULFONAMIDE COMPOUNDS WITH SELECTIVE ACTIVITY IN VOLTAGE-GATED SODIUM CHANNELS
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Page/Page column 0123, (2018/06/06)
Disclosed are compounds of Formula A, or a salt thereof: Formula (A), wherein: Het, Q and R1A to R4A are defined herein, which compounds have properties for blocking Nav 1.7 ion channels found in peripheral and sympathetic
Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 position
Rittle, Kenneth E.,Barrow, James C.,Cutrona, Kellie J.,Glass, Kristen L.,Krueger, Julie A.,Kuo, Lawrence C.,Lewis, S. Dale,Lucas, Bobby J.,McMasters, Daniel R.,Morrissette, Matthew M.,Nantermet, Philippe G.,Newton, Christina L.,Sanders, William M.,Yan, Youwei,Vacca, Joseph P.,Selnick, Harold G.
, p. 3477 - 3482 (2007/10/03)
Thrombin inhibitors incorporating o-aminoalkylbenzylamides in the P1 position were designed, synthesized and found to have enhanced potency and selectivity in several different structural classes. X-ray crystallographic analysis of compound 24 bound in the α-thrombin-hirugen complex provides an explanation for these unanticipated results.
