CID 3438253

Base Information

Chemical Name:CID 3438253
CAS No.:13473-51-3
Molecular Formula:C₃₅H₅₂O₁₅
Molecular Weight:712.789
Hs Code.:
Wikidata:Q104952088
Mol file:13473-51-3.mol

Synonyms:SCHEMBL868148

Suppliers and Price of CID 3438253

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

Total 4 raw suppliers

Chemical Property of CID 3438253

Chemical Property:

Boiling Point:927.8°Cat760mmHg
Flash Point:288.6°C
Density:1.5g/cm³
XLogP3:-2.3
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:7
Exact Mass:712.33062095
Heavy Atom Count:50
Complexity:1340

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)O)OC7C(C(C(C(O7)CO)O)O)O

Technology Process of CID 3438253

There total 5 articles about CID 3438253 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:

: C₃₈H₅₆O₁₅

: 7044-33-9,13473-51-3,54763-06-3,84123-19-3,89759-07-9
convalloside

Guidance literature:: With acetic acid; In ethanol; Yield given; Heating;
DOI:10.1007/BF00598579

Reference yield:

: 508-75-8,4336-94-1,5822-57-1,6147-48-4,6161-22-4,7553-98-2,38183-68-5,73208-83-0,73284-86-3,88195-71-5,90529-01-4,145107-75-1
convallatoxin

: 7044-33-9,13473-51-3,54763-06-3,84123-19-3,89759-07-9
convalloside

Guidance literature:: Multi-step reaction with 3 steps

1: 1.97 g / anhydrous copper sulfate / Heating

2: 1) silver carbonate, mercury oxide, HgO, 2) 0.3N sodium hydroxide / 1) chloroethane, dichloroethane, 30 min, reflux, 2) water, 18 deg C to 20 deg C, 30 min

3: 10percent aq. acetic acid / ethanol / Heating

With sodium hydroxide; copper(I) sulfate; acetic acid; silver carbonate; mercury(II) oxide; In ethanol;
DOI:10.1007/BF00598579

Reference yield:

: 69980-52-5
2,3,4-tri-O-acetyl-L-rhamnopyranosyl bromide

: 7044-33-9,13473-51-3,54763-06-3,84123-19-3,89759-07-9
convalloside

Guidance literature:: Multi-step reaction with 4 steps

1: 1) silver carbonate, mercury oxide, HgO, 2) 0.3N sodium hydroxide / 1) chloroethane, dichloroethane, 2) water

2: 1.97 g / anhydrous copper sulfate / Heating

3: 1) silver carbonate, mercury oxide, HgO, 2) 0.3N sodium hydroxide / 1) chloroethane, dichloroethane, 30 min, reflux, 2) water, 18 deg C to 20 deg C, 30 min

4: 10percent aq. acetic acid / ethanol / Heating

With sodium hydroxide; copper(I) sulfate; acetic acid; silver carbonate; mercury(II) oxide; In ethanol;
DOI:10.1007/BF00598579