60085-61-2

Usage

Uses

Used in Pharmaceutical Industry:
2-diethoxyethylcarbaMate is used as a muscle relaxant for managing severe muscle spasms and stiffness in patients with conditions such as cerebral palsy or other forms of severe spastic cerebral palsy. It operates by blocking the release of specific chemical messengers in the brain, which are responsible for muscle contractions and stiffness, thereby alleviating the symptoms and improving the quality of life for these individuals.
It is typically administered orally in the form of tablets or liquid suspension, with dosage determined based on the individual's age, weight, and the severity of their condition. However, caution is advised when using 2-diethoxyethylcarbaMate in people with liver or kidney problems due to potential complications. Common side effects of this medication may include drowsiness, dizziness, and muscle weakness. Overall, 2-diethoxyethylcarbaMate serves as an important and effective treatment option for managing severe muscle spasms and stiffness in certain medical conditions.

InChI:InChI=1/C14H21NO4/c1-3-17-13(18-4-2)10-15-14(16)19-11-12-8-6-5-7-9-12/h5-9,13H,3-4,10-11H2,1-2H3,(H,15,16)

Upstream product

• 645-36-3 2,2-diethoxy-ethanamine 
• 501-53-1 benzyl chloroformate 
• 113738-28-6 2-azidoethanal diethyl acetal 
• 621-62-5 chloroacetaldehyde diethyl acetal 

Downstream Products

• 76257-22-2 dimethyl 2-benzyloxycarbonylaminomethyl-1,3-dioxane-5,5-dicarboxylate 
• 79940-61-7 1,2,3,4-tetrahydro-1-((N-benzyloxycarbonylamino)methyl)-2-benzyl-β-carboline 
• 76245-18-6 methyl cis-2-benzyloxycarbonylaminomethyl-1,3-dioxane-5-carboxylate 
• 76245-17-5 methyl trans-2-benzyloxycarbonylaminomethyl-1,3-dioxane-5-carboxylate 
• 76245-20-0 cis-2-benzyloxycarbonylaminomethyl-1,3-dioxane-5-carboxylic acid 
• 76245-19-7 trans-2-benzyloxycarbonylaminomethyl-1,3-dioxane-5-carboxylic acid 
• 76245-16-4 2-(Benzyloxycarbonylamino-methyl)-[1,3]dioxane-5-carboxylic acid benzyl ester 
• 31236-63-2 [2-(2,4-dinitro-phenylhydrazono)-ethyl]-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis of substituted anilinesviaa gold-catalyzed three-component reaction

A three-component reaction for the synthesis of substituted anilines by a gold(i)-catalyzed domino reaction was developed. Cationic gold catalysts selectively and sequentially activated two different alkynes, which were involved in pyrrole synthesis and subsequent Diels-Alder reaction. The sequential formal (3 + 2) annulation/Diels-Alder reaction of three components provided a variety of substituted anilines in a modular fashion. Moreover, utility of the aniline products was demonstrated by derivatization to substituted benzoxazines, which are pharmaceutically important heterocycles.

CARBAMATE DERIVATIVES, PROCESS FOR PRODUCING THE SAME AND USE THEREOF

Novel carbamate derivatives which are useful as drugs because of inhibiting activated blood coagulation factor X and thus exerting an anticoagulant effect. Compounds represented by the formula: wherein R1 represents a group represented by the formula: (wherein Y1 represents CH=CH, etc.), which may be substituted, etc.; the ring A represents an oxo-substituted nitrogen-containing heterocyclic ring which may be further substituted; R2 represents a hydrogen atom, optionally substituted C1-4 alkyl, etc.; R3 represents optionally substituted C1-4 alkyl, etc.; and Z represents an optionally substituted nitrogen containing heterocyclic group, etc., or salts thereof.