13880-74-5 Usage
Uses
Used in Pharmaceutical Industry:
4-aminopentanoic acid is used as a drug for controlling bleeding by inhibiting the activity of enzymes that dissolve blood clots. This helps in the treatment of conditions that involve excessive bleeding or clotting disorders.
Used in Synthesis of Pharmaceuticals:
4-aminopentanoic acid is used as a building block in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into different drug molecules, contributing to the development of new medications.
Used as a Stabilizer for Biological Tissues and Cells:
4-aminopentanoic acid is used as a stabilizer for biological tissues and cells. Its ability to control bleeding and interact with enzymes makes it useful in preserving the integrity and function of biological samples in research and medical applications.
Used in Materials Science:
4-aminopentanoic acid has potential applications in the field of materials science, particularly in the development of polymeric materials and coatings. Its chemical properties can be utilized to create new materials with specific properties, such as improved strength, durability, or biocompatibility.
Check Digit Verification of cas no
The CAS Registry Mumber 13880-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13880-74:
(7*1)+(6*3)+(5*8)+(4*8)+(3*0)+(2*7)+(1*4)=115
115 % 10 = 5
So 13880-74-5 is a valid CAS Registry Number.
13880-74-5Relevant academic research and scientific papers
Ammonia borane enabled upgrading of biomass derivatives at room temperature
Meier, Sebastian,Riisager, Anders,Yang, Song,Zhao, Wenfeng
supporting information, p. 5972 - 5977 (2020/11/03)
Simplifying biomass conversion to valuable products with high efficiency is pivotal for the sustainable development of society. Herein, an efficient catalyst-free system using ammonia borane (AB) as the hydrogen donor is described, which enables controllable reaction selectivity towards four value-added products in excellent yield (82-100%) under very mild conditions. In particular, the system is uniquely efficient to produce γ-valerolactone (GVL) at room temperature. Combined in situ NMR and computational studies elucidate the hydrogen transfer mechanism of AB in methanol, the novel pathway of GVL formation from levulinate in water, and a competitive mechanism between reduction and reductive amination in the same system. Moreover, carbohydrates are converted directly into GVL in good yield, using a one-pot, two-step strategy. Products of a rather broad scope are prepared within a short reaction time of 30 min by using this catalyst-free strategy in methanol at room temperature. This journal is
