Lydimycin

Base Information

Chemical Name:Lydimycin
CAS No.:10118-85-1
Molecular Formula:C₁₀H₁₄N₂O₃S
Molecular Weight:242.299
Hs Code.:
UNII:U1E84J0228
DSSTox Substance ID:DTXSID40883091
Nikkaji Number:J9.657A,J92.753H
Wikidata:Q27290557
NCI Thesaurus Code:C90684
Metabolomics Workbench ID:144402
ChEMBL ID:CHEMBL3989616
Mol file:10118-85-1.mol

Synonyms:alpha-dehydrobiotin

Suppliers and Price of Lydimycin

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

American Custom Chemicals Corporation
LIDIMYCIN 95.00%
5MG
$ 499.76

Total 7 raw suppliers

Chemical Property of Lydimycin

Chemical Property:

Vapor Pressure:1.35E-15mmHg at 25°C
Boiling Point:593°Cat760mmHg
Flash Point:312.4°C
PSA：103.73000
Density:1.3g/cm³
LogP:1.23040
XLogP3:0.4
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:242.07251349
Heavy Atom Count:16
Complexity:332

Purity/Quality:

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

LIDIMYCIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2C(C(S1)CCC=CC(=O)O)NC(=O)N2
Isomeric SMILES:C1[C@H]2[C@@H]([C@@H](S1)CC/C=C/C(=O)O)NC(=O)N2
Uses Antifungal.

Technology Process of Lydimycin

There total 14 articles about Lydimycin 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:

: 27368-84-9,27368-88-3,60209-11-2
5-((3aS)-1,3-dibenzyl-2-oxo-(3ar,6ac)-hexahydro-thieno[3,4-d]imidazol-4t-yl)-pent-2t-enoic acid ethyl ester

: 10118-85-1
d-α-Dehydrobiotin

Guidance literature:: With phosphoric acid; phenol; at 150 ℃; for 3h;
DOI:10.1021/jo00886a017

Reference yield:

: 27512-85-2,29455-31-0
3-(1,3-dibenzyl-2-oxo-(3ar,6ac)-hexahydro-thieno[3,4-d]imidazol-4t-yl)-propionaldehyde

: 10118-85-1,27368-91-8
dl-α-Dehydrobiotin

Guidance literature:: Multi-step reaction with 3 steps

1: NaH / tetrahydrofuran

2: aq. HBr

3: aq. NaOH

With sodium hydroxide; hydrogen bromide; sodium hydride; In tetrahydrofuran;
DOI:10.1021/jo00886a017

Reference yield:

: 27368-83-8,27368-87-2
1,3-dibenzyl-4t-(3-hydroxy-propyl)-(3ar,6ac)-tetrahydro-thieno[3,4-d]imidazol-2-one

: 10118-85-1,27368-91-8
dl-α-Dehydrobiotin

Guidance literature:: Multi-step reaction with 4 steps

1: DMSO, DCC, Py, CF₃CO₂H

2: NaH / tetrahydrofuran

3: aq. HBr

4: aq. NaOH

With pyridine; sodium hydroxide; hydrogen bromide; sodium hydride; dimethyl sulfoxide; dicyclohexyl-carbodiimide; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1021/jo00886a017