6280-16-6 Usage
Uses
Used in Polymer and Copolymer Production:
N-Allyl-2-hydroxypropionamide is used as a monomer for the production of polymers and copolymers. Its unique structure allows for the creation of materials with enhanced properties, such as improved adhesion and water resistance.
Used in Adhesive and Coating Formulation:
N-Allyl-2-hydroxypropionamide is used as a crosslinking agent in the formulation of adhesives and coatings. Its presence helps to strengthen the bonds between molecules, resulting in more durable and long-lasting products.
Used in Specialty Chemical Synthesis:
N-Allyl-2-hydroxypropionamide serves as a precursor for the synthesis of specialty chemicals. Its versatile chemical structure makes it a valuable building block for the development of new and innovative compounds.
Used in Various Industries:
N-Allyl-2-hydroxypropionamide is utilized across a wide range of industries, including construction, automotive, and textiles, due to its ability to improve the performance and durability of various materials.
It is important to handle N-Allyl-2-hydroxypropionamide with care, as it may cause irritation to the skin and eyes, and should be used in well-ventilated areas.
Check Digit Verification of cas no
The CAS Registry Mumber 6280-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6280-16:
(6*6)+(5*2)+(4*8)+(3*0)+(2*1)+(1*6)=86
86 % 10 = 6
So 6280-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO2/c1-3-4-7-6(9)5(2)8/h3,5,8H,1,4H2,2H3,(H,7,9)
6280-16-6Relevant academic research and scientific papers
FORUMLATIONS
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Page/Page column 4, (2009/09/25)
This invention relates to the use of lactamide compounds of formula (I): CH3CH(OH)C(=O)NR1R2, where R1 and R2 are each independently hydrogen; or C1-6 alkyl, C2-6 alkenyl or C3-6 cycloalkyl, each of which is optionally substituted by up to three substituents independently selected from phenyl, hydroxy, C1-5 alkoxy, morpholinyl and NR3R4 where R3 and R4 are each independently C1-3 alkyl; or phenyl optionally substituted by up to three substituents independently selected from C1-3 alkyl; or R1 and R2 together with the nitrogen atom to which they are attached form a morpholinyl, pyrrolidinyl, piperidinyl or azepanyl ring, each of which is optionally substituted by up to three substituents independently selected from C1-3 alkyl, in formulations to reduce the toxicity associated with other formulation components; to the use of certain lactamide compounds as solvents, especially in formulations, particularly in agrochemical formulations and in environmentally friendly formulations; to novel lactamide compounds; and to processes for preparing lactamide compounds.
