Amiprilose

Base Information

Chemical Name:Amiprilose
CAS No.:56824-20-5
Molecular Formula:C₁₄H₂₇NO₆
Molecular Weight:305.371
Hs Code.:
European Community (EC) Number:633-482-1
UNII:S0FG5X68QT
Nikkaji Number:J22.171F
Wikidata:Q27288398
NCI Thesaurus Code:C76690
ChEMBL ID:CHEMBL1316321

Synonyms:1,2-O-isopropylidene-3-O-3'-(N',N'-dimethylamino-N-propyl)-D-glucofuranose;3-O-(3-(dimethylamino)propyl)-1,2-O-(1-methylethylidene)- alpha-D-glucofuranose;amiprilose;amiprilose hydrochloride;amprilose;SM 1213;SM-1213;Therafectin

Suppliers and Price of Amiprilose

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
AmipriloseHydrochloride
5mg
$ 65.00

Matrix Scientific
Amiprilose 95+%
1g
$ 1647.00

Matrix Scientific
Amiprilose 95+%
250mg
$ 742.00

Crysdot
Amiprilose 95+%
1g
$ 1240.00

Chemenu
AmipriloseHydrochloride 95%
1g
$ 1169.00

Biosynth Carbosynth
Amiprilose
1 g
$ 1500.00

Biosynth Carbosynth
Amiprilose
250 mg
$ 590.00

Biosynth Carbosynth
Amiprilose
100 mg
$ 375.00

Biosynth Carbosynth
Amiprilose
50 mg
$ 230.00

Biosynth Carbosynth
Amiprilose
500 mg
$ 950.00

Total 24 raw suppliers

Chemical Property of Amiprilose

Chemical Property:

Melting Point:255oC
Refractive Index:1.521
Boiling Point:431 °C at 760 mmHg
PKA:13.51±0.20(Predicted)
Flash Point:214.5 °C
PSA：80.62000
Density:1.21 g/cm³
LogP:0.35490
Storage Temp.:2-8°C
XLogP3:-0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:305.18383758
Heavy Atom Count:21
Complexity:337

Purity/Quality:

98%Min ^*data from raw suppliers

AmipriloseHydrochloride ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 23/24/25-36/37/38
Safety Statements: 22-26-36-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(OC2C(C(OC2O1)C(CO)O)OCCCN(C)C)C
Isomeric SMILES:CC1(O[C@@H]2[C@H]([C@H](O[C@@H]2O1)[C@@H](CO)O)OCCCN(C)C)C
Uses Anti-inflammatory.

Technology Process of Amiprilose

There total 3 articles about Amiprilose 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: 70.0%

: 53914-14-0
3-O-<3-(N,N-dimethylamino)propyl>-1,2,5,6-di-O-isopropylidene-α-D-glucofuranose

: 56824-20-5
3-O-<3-(N,N-dimethylamino)propyl>-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: With hydrogenchloride; Ambient temperature;

Reference yield:

: 5407-04-5
3-(dimethylamino)propyl chloride hydrochloride

: 56824-20-5
3-O-<3-(N,N-dimethylamino)propyl>-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / NaOH / dioxane / 12 h / Heating

2: 70 percent / aq. HCl / Ambient temperature

With hydrogenchloride; sodium hydroxide; In 1,4-dioxane;

Reference yield:

: 582-52-5
1,2:5,6-di-O-isopropylidene-α-D-glucofuranose

: 56824-20-5
3-O-<3-(N,N-dimethylamino)propyl>-1,2-O-isopropylidene-α-D-glucofuranose

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / NaOH / dioxane / 12 h / Heating

2: 70 percent / aq. HCl / Ambient temperature

With hydrogenchloride; sodium hydroxide; In 1,4-dioxane;