152970-08-6

Basic information

• Product Name: Propanamide, N-ethyl-2-hydroxy-, (R)- (9CI)
• Synonyms: Propanamide, N-ethyl-2-hydroxy-, (R)- (9CI)
• CAS NO: 152970-08-6
• Molecular Formula: C5H11NO2
• Molecular Weight: 117.14634
• Product Categories: ACETYLGROUP
• Mol File: 152970-08-6.mol

Chemical Properties

• Boiling Point: 280.9±23.0 °C(Predicted)
• Appearance: /
• Density: 1.019±0.06 g/cm3(Predicted)
• Solubility: Chloroform; Dichloromethane; DMF; Ethyl Acetate; Methanol
• PKA: 13.65±0.20(Predicted)
• CAS DataBase Reference: Propanamide, N-ethyl-2-hydroxy-, (R)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Propanamide, N-ethyl-2-hydroxy-, (R)- (9CI)(152970-08-6)
• EPA Substance Registry System: Propanamide, N-ethyl-2-hydroxy-, (R)- (9CI)(152970-08-6)

Safety Data

• Hazardous Substances Data: 152970-08-6(Hazardous Substances Data)

Usage

Uses

Used in Pesticide Detection:
Propanamide, N-ethyl-2-hydroxy-, (R)(9CI) is used as an intermediate in the synthesis of Carbetamide-D5, which is employed for the determination of pesticides. The compound aids in the accurate identification and quantification of pesticide residues in various samples, ensuring the safety and quality of agricultural products.
Used in Chemical Synthesis:
In the field of chemical synthesis, Propanamide, N-ethyl-2-hydroxy-, (R)(9CI) serves as a key component in the production of Carbetamide-D5. Propanamide, N-ethyl-2-hydroxy-, (R)(9CI) is essential for the development of new chemical products and contributes to the advancement of research and innovation in the chemical industry.

Upstream product

• 547-64-8 methyl lactate 
• 75-04-7 ethylamine 
• 22381-21-1 N,N-diethyl-2-oxo-propanamide 
• 687-47-8 (S)-Ethyl lactate 

Downstream Products

• 69374-80-7 N-ethyl pyruvamide 

Relevant articles and documents

FORUMLATIONS

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.

Enantioselective hydrogenation of α-ketoamides over Pt/A12O3 modified by cinchona alkaloids

Pyruvamide and its N-alkylated derivatives have been synthesised and hydrogenated enantioselectively to the corresponding alcohols over an alumina-supported Pt catalyst chirally modified by adsorbed cinchonidine. Depending on the substrate structure and r

PHOTOCHEMICAL REACTIONS OF alpha -OXO AMIDES. NORRISH TYPE II REACTIONS VIA ZWITTERIONIC INTERMEDIATES.

The mechanism of the photochemical reactions of alpha -oxo amides was studied. Establishment of the intermediacy zwitterions was accomplished by the detection of iminium ions formed by protonation of the zwitterions and by the independent generation of the zwitterions by the reaction of hydroxyphenylketene with imines. The remarkable substituent and solvent effects in the photoreactions were rationalized on the basis of the mechanism.