Betiatide

Base Information

Chemical Name:Betiatide
CAS No.:103725-47-9
Molecular Formula:C15H17 N3 O6 S
Molecular Weight:367.382
Hs Code.:
UNII:9NV2SR34P8
DSSTox Substance ID:DTXSID3048788
Nikkaji Number:J586.293K
Wikidata:Q27272797
NCI Thesaurus Code:C65261
RXCUI:194098
Metabolomics Workbench ID:154786
ChEMBL ID:CHEMBL3183117
Mol file:103725-47-9.mol

Synonyms:S-benzoyl-MAG3;S-benzoylmercaptoacetyltriglycine

Suppliers and Price of Betiatide

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
BETIATIDE 95.00%
25MG
$ 997.50

American Custom Chemicals Corporation
BETIATIDE 95.00%
5MG
$ 502.69

Total 10 raw suppliers

Chemical Property of Betiatide

Chemical Property:

Vapor Pressure:6.73E-27mmHg at 25°C
Melting Point:193-195 °C (decomp)(Solv: isopropanol (67-63-0))
Boiling Point:798.5 °C at 760 mmHg
PKA:3.32±0.10(Predicted)
Flash Point:436.7 °C
PSA：166.97000
Density:1.397 g/cm³
LogP:0.16590
XLogP3:-0.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:10
Exact Mass:367.08380644
Heavy Atom Count:25
Complexity:519

Purity/Quality:

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

BETIATIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)SCC(=O)NCC(=O)NCC(=O)NCC(=O)O
Uses Pharmaceutic aid.

Technology Process of Betiatide

There total 6 articles about Betiatide 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: 82.0%

: 556-33-2
glycine-glycine-glycine

: 90236-37-6
succinimidyl-S-benzoylthioglycolate

: 103725-47-9
benzoylmercaptoacetylglycylglycylglycine

Guidance literature:: With sodium hydroxide; In acetonitrile; at 20 - 60 ℃; for 6h;

Reference yield:

: 98-91-9
thiobenzoic acid

: 104186-69-8
2-{2-[2-(2-chloroacetamido)acetamido]acetamido}acetic acid

: 103725-47-9
benzoylmercaptoacetylglycylglycylglycine

Guidance literature:: In methanol;
DOI:10.1016/j.bmcl.2009.03.059 DOI:10.1016/j.bmcl.2010.03.003

Reference yield:

: 6398-74-9
S-benzoylthioglycolic acid

: 103725-47-9
benzoylmercaptoacetylglycylglycylglycine

Guidance literature:: Multi-step reaction with 2 steps

1: 1,3-dicyclohexylcarbodiimide / tetrahydrofuran

2: NaOH / H₂O / 2.5 h / Heating

With sodium hydroxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; water;
DOI:10.1002/jlcr.897