6-Nitrotryptophan

Base Information

Chemical Name:6-Nitrotryptophan
CAS No.:46885-76-1
Molecular Formula:C11H11 N3 O4
Molecular Weight:249.226
Hs Code.:
DSSTox Substance ID:DTXSID20196974
Nikkaji Number:J444.006D
Wikidata:Q83069950
ChEMBL ID:CHEMBL1620859
Mol file:46885-76-1.mol

Synonyms:6-nitrotryptophan;tryptophan, 6-nitro-

Suppliers and Price of 6-Nitrotryptophan

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 22 raw suppliers

Chemical Property of 6-Nitrotryptophan

Chemical Property:

Vapor Pressure:2.91E-12mmHg at 25°C
Boiling Point:534.7°Cat760mmHg
Flash Point:277.2°C
PSA：124.93000
Density:1.541g/cm³
LogP:2.25400
XLogP3:-1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:249.07495584
Heavy Atom Count:18
Complexity:344

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1[N+](=O)[O-])NC=C2CC(C(=O)O)N
Isomeric SMILES:C1=CC2=C(C=C1[N+](=O)[O-])NC=C2C[C@@H](C(=O)O)N

Technology Process of 6-Nitrotryptophan

There total 5 articles about 6-Nitrotryptophan 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: 91.0%

: 4769-96-4
6-nitroindole

: 56-45-1,83245-15-2
L-serin

: 46885-76-1
6-nitro-L-tryptophan

Guidance literature:: With Pf₀A₉ E₁₀₄G enzyme; In aq. phosphate buffer; water; dimethyl sulfoxide; at 75 ℃; for 12h; pH=8; Reagent/catalyst; Enzymatic reaction;
DOI:10.1021/jacs.7b05007

Reference yield:

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 46885-76-1
6-nitro-L-tryptophan

Guidance literature:: With nitric acid; acetic acid;
DOI:10.1021/ol902944f DOI:10.1071/CH10033

Reference yield:

: 105902-18-9
N^α-acetyl-6-nitro-D,L-tryptophan

: 1029430-16-7
N^α-acetyl-6-nitro-D-tryptophan

: 46885-76-1
6-nitro-L-tryptophan

: 56937-50-9
6-nitro-D-tryptophan

: 105902-18-9
N^α-acetyl-6-nitro-L-tryptophan

Guidance literature:: With borate buffer; cobalt(II) chloride; at 37 ℃; for 48h; pH=8.0; Title compound not separated from byproducts.; Enzymatic reaction;
DOI:10.1016/j.tetlet.2008.02.120