77172-36-2 Usage
Uses
Used in Organic Synthesis:
TERT-BUTYL (3-AMINO-3-IMINOPROPYL)CARBAMATE is used as a reactive intermediate in organic synthesis for its capacity to participate in a wide range of chemical reactions, facilitating the creation of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, TERT-BUTYL (3-AMINO-3-IMINOPROPYL)CARBAMATE is utilized as a key component in the development of new drugs, leveraging its reactivity and metal-complexing properties to enhance drug efficacy and delivery.
Used in Catalysis:
TERT-BUTYL (3-AMINO-3-IMINOPROPYL)CARBAMATE is employed as a catalyst or catalyst precursor in various chemical processes due to its ability to form stable complexes with metals, which can accelerate reaction rates and improve yields.
Used in Drug Delivery Systems:
TERT-BUTYL (3-AMINO-3-IMINOPROPYL)CARBAMATE is used as a component in drug delivery systems to improve the bioavailability and targeting of therapeutic agents, potentially enhancing the effectiveness and safety of medications.
Used in Material Science:
In the field of material science, TERT-BUTYL (3-AMINO-3-IMINOPROPYL)CARBAMATE serves as a building block for designing new materials with unique properties, such as high stability, reactivity, or specific catalytic functions.
Check Digit Verification of cas no
The CAS Registry Mumber 77172-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,7 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77172-36:
(7*7)+(6*7)+(5*1)+(4*7)+(3*2)+(2*3)+(1*6)=142
142 % 10 = 2
So 77172-36-2 is a valid CAS Registry Number.
77172-36-2Relevant academic research and scientific papers
Acylation of Dibasic Compounds Containing Amino Amidine and Aminoguanidine Functions
Barker, Peter L.,Gendler, Paul L.,Rapoport, Henry
, p. 2455 - 2465 (2007/10/02)
The site of acylation in difunctional compounds containing an amine and either an amidine or guanidine can be determined from the ultraviolet absorption spectrum of the acylated product.If the amidine or guanidine has been acylated, the product possesses a chromophore that is pH dependent, whereas if an amide was formed, the chromophore is independent of pH.
