51977-18-5 Usage
Uses
Used in Chemical Synthesis:
2-(propan-2-ylamino)butan-1-ol is used as a building block for the synthesis of other organic compounds due to its versatile chemical structure and reactivity.
Used in Pharmaceutical Industry:
2-(propan-2-ylamino)butan-1-ol is used as a chemical intermediate for the production of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(propan-2-ylamino)butan-1-ol is utilized as a chemical intermediate, playing a role in the formulation of various agrochemical products.
Used as a Solvent:
2-(propan-2-ylamino)butan-1-ol is employed as a solvent in various chemical processes, taking advantage of its ability to dissolve a wide range of substances.
Used as a Surfactant:
2-(propan-2-ylamino)butan-1-ol is also used as a surfactant in industrial applications, where its properties help to reduce surface tension and stabilize mixtures.
Used in Research and Development:
2-(propan-2-ylamino)butan-1-ol is utilized in research and development settings for the exploration of new chemical reactions and the creation of novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 51977-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,7 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51977-18:
(7*5)+(6*1)+(5*9)+(4*7)+(3*7)+(2*1)+(1*8)=145
145 % 10 = 5
So 51977-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H17NO/c1-4-7(5-9)8-6(2)3/h6-9H,4-5H2,1-3H3
51977-18-5Relevant academic research and scientific papers
Aluminium triflate: an efficient recyclable Lewis acid catalyst for the aminolysis of epoxides
Williams, D. Bradley G.,Lawton, Michelle
, p. 6557 - 6560 (2007/10/03)
Epoxides are powerful starting materials for a range of useful materials and can be converted into, amongst others, amino alcohols. In this work, a range of epoxides was ring-opened using various alkyl- and arylamines under the action of aluminium triflat
