Eucatropine

Base Information

• Chemical Name: Eucatropine
• CAS No.: 100-91-4
• Molecular Formula: C17H25 N O3
• Molecular Weight: 291.39
• European Community (EC) Number: 202-900-0
• UNII: 4SPJ105W8E
• DSSTox Substance ID: DTXSID1048465
• Nikkaji Number: J4.987E
• Wikidata: Q27166212
• NCI Thesaurus Code: C166782
• ChEMBL ID: CHEMBL1618660
• Mol file: 100-91-4.mol

Synonyms:eucatropine;Euphthalmine;100-91-4;eucatropin;Eucatropina;Eucatropinum;Eucatropine [INN:BAN];Eucatropinum [INN-Latin];Eucatropina [INN-Spanish];euphthalmin;UNII-4SPJ105W8E;4SPJ105W8E;(1,2,2,6-tetramethylpiperidin-4-yl) 2-hydroxy-2-phenylacetate;EINECS 202-900-0;Benzeneacetic acid, .alpha.-hydroxy-, 1,2,2,6-tetramethyl-4-piperidinyl ester;eucatropin-;Eucatropine dl-form;Prestwick0_000794;Prestwick1_000794;Prestwick2_000794;Prestwick3_000794;EUCATROPINE [INN];BSPBio_000928;SCHEMBL132347;SPBio_002867;BPBio1_001022;CHEMBL1618660;DTXSID1048465;BDBM82377;CHEBI:94371;EUCATROPINE DL-FORM [MI];NSC_7534;NCGC00179372-01;CAS_100-91-4;HY-117284;1,2,2,6-Tetramethyl-4-piperidyl mandelate;CS-0064980;FT-0712100;beta-1,2,2,6-tetramethyl-4-piperidinol mandelate;L000976;BRD-A37942872-003-03-2;Q27166212;4-HYDROXY-1,2,2,6-TETRAMETHYLPIPERIDINE MANDELATE;mandelic acid beta-1,2,2,6-tetramethyl-4-piperidyl ester;1,2,2,6-Tetramethyl-4-piperidinyl hydroxy(phenyl)acetate #;1,2,2,6-tetramethylpiperidin-4-yl 2-hydroxy-2-phenylacetate;MANDELIC ACID, 1,2,2,6-TETRAMETHYL-4-PIPERIDYL ESTER;2-hydroxy-2-phenylacetic acid (1,2,2,6-tetramethyl-4-piperidinyl) ester;alpha-Hydroxybenzeneacetic acid 1,2,2,6-tetramethyl-4-piperidinyl ester;Benzeneacetic acid, alpha-hydroxy-, 1,2,2,6-tetramethyl-4-piperidinyl ester

Chemical Property of Eucatropine

Chemical Property:

• Vapor Pressure: 9.97E-08mmHg at 25°C
• Boiling Point: 388.7°Cat760mmHg
• Flash Point: 188.8°C
• PSA: 49.77000
• Density: 1.11g/cm³
• LogP: 2.46240
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 291.18344366
• Heavy Atom Count: 21
• Complexity: 363

Purity/Quality:

98%,99%, ^*data from raw suppliers

EUCATROPINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1CC(CC(N1C)(C)C)OC(=O)C(C2=CC=CC=C2)O
• Uses: Anticholinergic.

Technology Process of Eucatropine

There total 2 articles about Eucatropine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

MANDELIC ACID (611-71-2,611-72-3,17199-29-0,90-64-2) → (+/-)-mandelic acid-(1,2,2,6t-tetramethyl-[4r]piperidyl ester) (100-91-4)

Guidance literature:

With hydrogenchloride;

Reference yield:

MANDELIC ACID (611-71-2,611-72-3,17199-29-0,90-64-2) → (+/-)-mandelic acid-(1,2,2,6c-tetramethyl-[4r]piperidyl ester) (100-91-4)

Guidance literature:

With hydrogenchloride;

upstream raw materials:

MANDELIC ACID