Fmoc-O-benzyl-L-tyrosyl chloride

Base Information

Chemical Name:Fmoc-O-benzyl-L-tyrosyl chloride
CAS No.:103321-60-4
Molecular Formula:C31H26ClNO4
Molecular Weight:512.005
Hs Code.:
DSSTox Substance ID:DTXSID201117204
Nikkaji Number:J1.053.006G
Mol file:103321-60-4.mol

Synonyms:103321-60-4;FMOC-O-BENZYL-L-TYROSYL CHLORIDE;Fmoc-Tyr(Bzl)-Cl;9H-fluoren-9-ylmethyl N-[(2S)-1-chloro-1-oxo-3-(4-phenylmethoxyphenyl)propan-2-yl]carbamate;Fmoc-O-Bzl-L-Tyr-OH chloride;(S)-(9H-Fluoren-9-yl)methyl (3-(4-(benzyloxy)phenyl)-1-chloro-1-oxopropan-2-yl)carbamate;GKHIGWPLGJZONE-LJAQVGFWSA-N;DTXSID201117204;FMOC-O-BENZYL-L-TYROSYLCHLORIDE;(S)-(9H-fluoren-9-yl)methyl 3-(4-(benzyloxy)phenyl)-1-chloro-1-oxopropan-2-ylcarbamate;(S)-(9H-Fluoren-9-yl)methyl(3-(4-(benzyloxy)phenyl)-1-chloro-1-oxopropan-2-yl)carbamate;9H-Fluoren-9-ylmethyl N-[(1S)-2-chloro-2-oxo-1-[[4-(phenylmethoxy)phenyl]methyl]ethyl]carbamate

Suppliers and Price of Fmoc-O-benzyl-L-tyrosyl chloride

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

TRC
Fmoc-Tyr(Bzl)-Cl
50mg
$ 60.00

American Custom Chemicals Corporation
FMOC-O-BENZYL-L-TYROSYL CHLORIDE 95.00%
5MG
$ 499.14

Total 3 raw suppliers

Chemical Property of Fmoc-O-benzyl-L-tyrosyl chloride

Chemical Property:

PSA：64.63000
LogP:6.87170
Storage Temp.:Store at 0°C
XLogP3:7.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:10
Exact Mass:511.1550360
Heavy Atom Count:37
Complexity:726

Purity/Quality:

98%min ^*data from raw suppliers

Fmoc-Tyr(Bzl)-Cl ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC=C(C=C2)CC(C(=O)Cl)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
Isomeric SMILES:C1=CC=C(C=C1)COC2=CC=C(C=C2)C[C@@H](C(=O)Cl)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
Uses Fmoc-Tyr(Bzl)-Cl is used as a reactant in the synthesis of sterically-hindered peptides.

Technology Process of Fmoc-O-benzyl-L-tyrosyl chloride

There total 1 articles about Fmoc-O-benzyl-L-tyrosyl chloride 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: 91.2%