Fmoc-Asp(OBzl)-OH

Base Information Edit

Chemical Name:Fmoc-Asp(OBzl)-OH
CAS No.:86060-84-6
Molecular Formula:C₂₆H₂₃NO₆
Molecular Weight:445.472
Hs Code.:29242990
European Community (EC) Number:692-002-9
DSSTox Substance ID:DTXSID50553435
Nikkaji Number:J1.697.235E
Wikidata:Q72478018
Mol file:86060-84-6.mol

Synonyms:Fmoc-Asp(OBzl)-OH;86060-84-6;Fmoc-L-aspartic acid 4-benzyl ester;L-Fmoc-aspartic acid beta-benzyl ester;n-alpha-fmoc-l-aspartic acid beta-benzyl ester;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(benzyloxy)-4-oxobutanoic acid;(2S)-4-(benzyloxy)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoic acid;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxo-4-phenylmethoxybutanoic acid;MFCD00065630;N-Fmoc-L-aspartic Acid beta-Benzyl Ester;Fmoc-L-aspartic acid b-benzyl ester;Fmoc-L-Asp(OBn);FMOC-Asp(OBzl);Fmoc-Asp(OBzl )-OH;4-Benzyl N-Fmoc-L-aspartate;SCHEMBL119962;DTXSID50553435;OQGAELAJEGGNKG-QHCPKHFHSA-N;AKOS015895331;AKOS015922806;CS-W002301;HY-W002301;L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-(phenylmethyl) ester;N-Fmoc-L-aspartic Acid 4-Benzyl Ester;AS-14267;B3887;Fmoc-Asp(OBzl)-OH, >=98.0% (HPLC);EN300-207179;J-300074;Q-101798;4-Benzyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic Acid 4-Benzyl Ester;(2S)-4-(benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid;(s)-2-(((9h-fluoren-9-yl)methoxy)carbonylamino)-4-(benzyloxy)-4-oxobutanoic acid;(2S)-4-(Benzyloxy)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid (non-preferred name)

Suppliers and Price of Fmoc-Asp(OBzl)-OH

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
Fmoc-L-aspartic acid beta-benzyl ester
5g
$ 366.00

TRC
Fmoc-asp(obzl)-oh
1g
$ 55.00

TCI Chemical
4-Benzyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate >98.0%(HPLC)(T)
25g
$ 264.00

TCI Chemical
4-Benzyl N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartate >98.0%(HPLC)(T)
5g
$ 53.00

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH Novabiochem?
25 g
$ 377.00

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH Novabiochem?
5 g
$ 93.90

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH Novabiochem . CAS 86060-84-6, molar mass 445.46 g/mol., Novabiochem
8520040005
$ 90.70

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH ≥98.0% (HPLC)
5 g
$ 82.70

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH Novabiochem . CAS 86060-84-6, molar mass 445.46 g/mol., Novabiochem
8520040025
$ 364.00

Sigma-Aldrich
Fmoc-Asp(OBzl)-OH ≥98.0% (HPLC)
5g-f
$ 135.00

Total 91 raw suppliers

Chemical Property of Fmoc-Asp(OBzl)-OH Edit

Chemical Property:

Appearance/Colour:white to light yellow crystal powder
Vapor Pressure:7.91E-20mmHg at 25°C
Melting Point:120-130 °C
Refractive Index:1.62
Boiling Point:120-130 °C
PKA:3.54±0.23(Predicted)
Flash Point:369.4 °C
PSA：101.93000
Density:1.31 g/cm³
LogP:4.50270
Storage Temp.:2-8°C
Solubility.:Soluble in methanol.
XLogP3:4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:10
Exact Mass:445.15253745
Heavy Atom Count:33
Complexity:668

Purity/Quality:

99% ^*data from raw suppliers

Fmoc-L-aspartic acid beta-benzyl ester ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 22-24/25

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)CC(C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24
Isomeric SMILES:C1=CC=C(C=C1)COC(=O)C[C@@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Technology Process of Fmoc-Asp(OBzl)-OH

There total 7 articles about Fmoc-Asp(OBzl)-OH 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: 81.0%