N-[(tert-Butoxy)carbonyl]-D-tryptophan

Base Information Edit

Chemical Name:N-[(tert-Butoxy)carbonyl]-D-tryptophan
CAS No.:5241-64-5
Molecular Formula:C16H20N2O4
Molecular Weight:304.346
Hs Code.:29339900
European Community (EC) Number:226-042-1
DSSTox Substance ID:DTXSID00200427
Nikkaji Number:J297.955A
Wikidata:Q72510535
Metabolomics Workbench ID:143430
ChEMBL ID:CHEMBL65670
Mol file:5241-64-5.mol

Synonyms:Boc-D-Trp-OH;5241-64-5;N-[(tert-Butoxy)carbonyl]-D-tryptophan;N-Boc-D-tryptophan;N-(tert-Butoxycarbonyl)-D-tryptophan;BOC-D-TRYPTOPHAN;(2R)-3-(1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;BOC-D-TRP;N-((tert-Butoxy)carbonyl)-D-tryptophan;CHEMBL65670;D-TRYPTOPHAN, N-[(1,1-DIMETHYLETHOXY)CARBONYL]-;EINECS 226-042-1;(R)-2-tert-Butoxycarbonylamino-3-(1H-indol-3-yl)-propionic acid;Nalpha-Boc-D-tryptophan;MFCD00037944;(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(1H-indol-3-yl)propanoic acid;Boc-D-TrpOH;Boc-DTrp-OH;BOC-(D)Trp-OH;N-|A-Boc-D-Tryptophan;N(alpha)-Boc-D-tryptophan;TERT-BUTOXYCARBONYL-;t-butoxycarbonyl-D-tryptophan;SCHEMBL1486167;DTXSID00200427;N-tert-Butoxycarbonyl-D-tryptophan;N-(t-Butoxycarbonyl)-D-tryptophan;CS-D1607;BDBM50043815;ZB0885;AKOS015922811;AC-1394;AM82278;(TERT-BUTOXYCARBONYL)-D-TRYPTOPHAN;AC-23659;AS-63540;Boc-D-Trp-OH, >=98.0% (TLC);B2259;EN300-154396;H12002;M03330;J-300266;N-alpha-t-Butyloxycarbonyl-D-tryptophane (Boc-D-Trp-OH);Z1070060900;(R)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(1H-INDOL-3-YL)PROPANOIC ACID

Suppliers and Price of N-[(tert-Butoxy)carbonyl]-D-tryptophan

Supply Marketing:Edit

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

Usbiological
N-alpha-Boc-D-tryptophan
25g
$ 359.00

TRC
Nα-Boc-D-tryptophan
50g
$ 375.00

TRC
Nα-Boc-D-tryptophan
25g
$ 250.00

TCI Chemical
N-(tert-Butoxycarbonyl)-D-tryptophan >98.0%(HPLC)
5g
$ 110.00

TCI Chemical
N-(tert-Butoxycarbonyl)-D-tryptophan >98.0%(HPLC)
1g
$ 28.00

Sigma-Aldrich
Boc-D-Trp-OH ≥98.0% (TLC)
5g
$ 53.80

Sigma-Aldrich
Boc-D-Trp-OH Novabiochem?
25 g
$ 49.90

Sigma-Aldrich
Boc-D-Trp-OH Novabiochem . CAS 5241-64-5, molar mass 304.34 g/mol., Novabiochem
8530860025
$ 48.20

Iris Biotech GmbH
Boc-D-Trp-OH
100 g
$ 438.75

Iris Biotech GmbH
Boc-D-Trp-OH
25 g
$ 148.50

Total 96 raw suppliers

Chemical Property of N-[(tert-Butoxy)carbonyl]-D-tryptophan Edit

Chemical Property:

Appearance/Colour:White to cream powder
Vapor Pressure:2.63E-12mmHg at 25°C
Melting Point:131-136 °C
Refractive Index:1.5800 (estimate)
Boiling Point:535.683 °C at 760 mmHg
PKA:4.00±0.10(Predicted)
Flash Point:277.771 °C
PSA：91.42000
Density:1.262 g/cm³
LogP:3.07920
Storage Temp.:-20°C
Solubility.:Aqueous Base (Slightly), DMF (Slightly) DMSO (Slightly), Methanol (Slightly)
XLogP3:2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:304.14230712
Heavy Atom Count:22
Complexity:419

Purity/Quality:

99% ^*data from raw suppliers

N-alpha-Boc-D-tryptophan ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O
Isomeric SMILES:CC(C)(C)OC(=O)N[C@H](CC1=CNC2=CC=CC=C21)C(=O)O
Uses Nα-Boc-D-tryptophan is an N-Boc-protected form of D-Tryptophan (T947205). D-Tryptophan is an unnatural isomer of L-Tryptophan (T947210) and is classified as an essential amino acid. D-Tryptophan has been synthesized as part of some potent Oxytocin (Acetate: O878500) antagonists that treat preterm labour.

Technology Process of N-[(tert-Butoxy)carbonyl]-D-tryptophan

There total 9 articles about N-[(tert-Butoxy)carbonyl]-D-tryptophan 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: 99.0%