5665-74-7 Usage
Description
DL-2-AMINO-1-HEXANOL, also known as DL-2-amino-1-hexanol, is an organic compound with a hexanol backbone and an amino group. It has been studied for its reduced mobility of protonated form in air at high temperatures, such as 200°C, using ion mobility spectrometry (IMS). DL-2-AMINO-1-HEXANOL has potential applications in various industries due to its unique chemical properties.
Uses
Used in Chemical Synthesis:
DL-2-AMINO-1-HEXANOL is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its versatile structure allows for the creation of a wide range of molecules with different functionalities, making it a valuable component in the development of new drugs and chemicals.
Used in Pharmaceutical Industry:
DL-2-AMINO-1-HEXANOL is used as an intermediate in the production of pharmaceuticals. Its unique structure and reactivity make it a suitable candidate for the development of new drugs with specific therapeutic properties.
Used in Cosmetics Industry:
DL-2-AMINO-1-HEXANOL is used as a component in the formulation of cosmetics, particularly in personal care products. Its properties may contribute to the development of products with improved skin compatibility and enhanced efficacy.
Used in Research and Development:
DL-2-AMINO-1-HEXANOL is used as a research compound for studying its properties and potential applications in various fields. The ion mobility spectrometry (IMS) studies at high temperatures provide valuable insights into its behavior and reactivity, which can be applied to develop new technologies and products.
Check Digit Verification of cas no
The CAS Registry Mumber 5665-74-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5665-74:
(6*5)+(5*6)+(4*6)+(3*5)+(2*7)+(1*4)=117
117 % 10 = 7
So 5665-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H15NO/c1-2-3-4-6(7)5-8/h6,8H,2-5,7H2,1H3
5665-74-7Relevant articles and documents
A catalyst-free, convenient construction of eight-membered [1,4]oxazocane-5,8-dione heterocycles from aminoethanols with divinyl succinate
Chen, Wan-Qin,Zhang, Qing-Yi,Liu, Bo-Kai,Wu, Qi,Lin, Xian-Fu
scheme or table, p. 1829 - 1832 (2009/04/07)
A convenient protocol for the synthesis of [1,4]oxazocane-5,8-dione heterocycles by direct cyclization using 2-substituted aminoethanols and divinyl succinate without any catalysts and additives was established. This strategy is quite simple and effective to obtain eight-membered rings incorporating lactone and lactam functional groups. Georg Thieme Verlag Stuttgart.
