Levamlodipine gentisate

Base Information

Chemical Name:Levamlodipine gentisate
CAS No.:856256-16-1
Molecular Formula:C₇H₆O₄*C₂₀H₂₅ClN₂O₅
Molecular Weight:563.004
Hs Code.:
UNII:4X8086K40B
Wikidata:Q27260630

Synonyms:Levamlodipine gentisate;856256-16-1;(s)-amlodipine gentisate;(s)-(-)-amlodipine gentisate;4X8086K40B;UNII-4X8086K40B;3,5-Pyridinedicarboxylic acid, 2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, (4S)-, 2,5-dihydroxybenzoate (1:1);2,5-dihydroxybenzoic acid;3-O-ethyl 5-O-methyl (4S)-2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate;3,5-Pyridinedicarboxylic acid, 2-[(2-aminoethoxy)methyl]-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-, 3-ethyl 5-methyl ester, (4S)-, 2,5-dihydroxybenzoate (1:1);3-ethyl 5-methyl (S)-2-((2-aminoethoxy)methyl)-4-(2-chlorophenyl)-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate 2,5-dihydroxybenzoate;SCHEMBL1379490;AKOS040747061;Q27260630

Suppliers and Price of Levamlodipine gentisate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Levamlodipine gentisate

Chemical Property:

Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:11
Exact Mass:562.1718083
Heavy Atom Count:39
Complexity:803

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)C1=C(NC(=C(C1C2=CC=CC=C2Cl)C(=O)OC)C)COCCN.C1=CC(=C(C=C1O)C(=O)O)O
Isomeric SMILES:CCOC(=O)C1=C(NC(=C([C@@H]1C2=CC=CC=C2Cl)C(=O)OC)C)COCCN.C1=CC(=C(C=C1O)C(=O)O)O

Technology Process of Levamlodipine gentisate

There total 2 articles about Levamlodipine gentisate 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: 92.0%

: (S)-(-)-amlodipine-hemi-dibenzoyl-D-tartrate

: 490-79-9
2,5-dihydroxybenzoic acid.

: 856256-16-1
S-amlodipine gentisate

Guidance literature:: (S)-(-)-amlodipine-hemi-dibenzoyl-D-tartrate; With sodium hydroxide; In dichloromethane; water; for 0.5h;

2,5-dihydroxybenzoic acid.; In dichloromethane; acetone; at 20 ℃; for 2h;

Reference yield: 92.0%

: (S)-(-)-amlodipine-hemi-dibenzoyl-D-tartrate

: 490-79-9
2,5-dihydroxybenzoic acid.

: 856256-16-1
S-amlodipine gentisate

Guidance literature:: (S)-(-)-amlodipine-hemi-dibenzoyl-D-tartrate; With sodium hydroxide; In dichloromethane; water; for 0.5h;

2,5-dihydroxybenzoic acid.; In dichloromethane; acetone; at 20 ℃; for 2h;