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Acyl carrier protein (65-74)

Base Information
  • Chemical Name:Acyl carrier protein (65-74)
  • CAS No.:66851-75-0
  • Molecular Formula:C47H74N12O16
  • Molecular Weight:1063.18
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90216976
  • Nikkaji Number:J402.323D
  • Wikidata:Q83093318
Acyl carrier protein (65-74)

Synonyms:ACP (65-74);acyl carrier protein (65-74)

Suppliers and Price of Acyl carrier protein (65-74)
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 5 raw suppliers
Chemical Property of Acyl carrier protein (65-74)
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:1574.4°Cat760mmHg 
  • PKA:3.27±0.10(Predicted) 
  • Flash Point:906°C 
  • PSA:468.93000 
  • Density:1.301g/cm3 
  • LogP:1.36380 
  • Storage Temp.:?20°C 
  • XLogP3:-4.4
  • Hydrogen Bond Donor Count:15
  • Hydrogen Bond Acceptor Count:17
  • Rotatable Bond Count:33
  • Exact Mass:1062.53457432
  • Heavy Atom Count:75
  • Complexity:2050
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC(C)C(C(=O)NC(CC(=O)O)C(=O)NC(CC1=CC=C(C=C1)O)C(=O)NC(C(C)CC)C(=O)NC(CC(=O)N)C(=O)NCC(=O)O)NC(=O)C(C)NC(=O)C(C)NC(=O)C(CCC(=O)N)NC(=O)C(C(C)C)N
  • Isomeric SMILES:CC[C@H](C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC1=CC=C(C=C1)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC(=O)N)C(=O)NCC(=O)O)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CCC(=O)N)NC(=O)[C@H](C(C)C)N
Technology Process of Acyl carrier protein (65-74)

There total 10 articles about Acyl carrier protein (65-74) 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:
Guidance literature:
C17H13NO10S2(2-)*2Na(1+); With sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; ethyl cyanoglyoxylate-2-oxime; In water; acetonitrile; at 20 ℃; for 0.416667h;
With piperazine; In water; for 0.166667h;
C20H18N2O11S2(2-)*2Na(1+); C21H21NO10S2(2-)*2Na(1+); C24H19NO11S2(2-)*2Na(1+); C20H19NO10S2(2-)*2Na(1+); C18H15NO10S2(2-)*2Na(1+); C19H16N2O11S2(2-)*2Na(1+); C23H23NO12S2(2-)*2Na(1+); Further stages;
DOI:10.1002/anie.202003676
Guidance literature:
With further Fmoc-amino-acid pentafluorophenyl esters; solid phase peptide synthesis on an amino resin;
DOI:10.1016/S0040-4020(01)86121-4
Guidance literature:
N-(fluoren-9-ylmethoxycarbonyl)glycine; With N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 2h; 2-CTC resin
With piperidine; In dichloromethane; N,N-dimethyl-formamide; for 0.333333h; 2-CTC resin
Fmoc-Val-OH; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine; Fmoc-Ile-OH; Fmoc-Asn(PG)-OH; Fmoc-Tyr(PG)-OH; Fmoc-Asp(PG)-OH; Fmoc-Gln(PG)-OH; Further stages;
DOI:10.1021/jacs.1c04614
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