BOC-D-ASP-OFM

Base Information

Chemical Name:BOC-D-ASP-OFM
CAS No.:214630-04-3
Molecular Formula:C23H25 N O6
Molecular Weight:411.455
Hs Code.:
Mol file:214630-04-3.mol

Synonyms:N-ALPHA-T-BUTOXYCARBONYL-D-ASPARTIC ACID ALPHA-9-FLUORENYLMETHYL ESTER;BOC-D-ASP-OFM;BOC-D-ASPARTIC ACID ALPHA-9-FLUORENYLMETHYL ESTER;BOC-D-ASPARTIC ACID-OFM

Suppliers and Price of BOC-D-ASP-OFM

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

Biosynth Carbosynth
Boc-D-Asp-OFm
2 g
$ 394.00

Biosynth Carbosynth
Boc-D-Asp-OFm
1 g
$ 227.00

Biosynth Carbosynth
Boc-D-Asp-OFm
500 mg
$ 130.00

Biosynth Carbosynth
Boc-D-Asp-OFm
10 g
$ 1368.70

Biosynth Carbosynth
Boc-D-Asp-OFm
5 g
$ 787.00

American Custom Chemicals Corporation
BOC-D-ASP-OFM 95.00%
5MG
$ 497.50

Total 9 raw suppliers

Chemical Property of BOC-D-ASP-OFM

Chemical Property:

Boiling Point:617.4±55.0 °C(Predicted)
PKA:4.01±0.19(Predicted)
PSA：101.93000
Density:1.251±0.06 g/cm3(Predicted)
LogP:4.10100
Storage Temp.:2-8°C

Purity/Quality:

98%Min ^*data from raw suppliers

Boc-D-Asp-OFm ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of BOC-D-ASP-OFM

There total 2 articles about BOC-D-ASP-OFM 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:

: 13726-67-5,62396-48-9,120341-32-4
N^α-(tert-butyloxycarbonyl)-D-aspartic acid

: 214630-04-3
(R)-2-tert-Butoxycarbonylamino-succinic acid 1-(9H-fluoren-9-ylmethyl) ester

Guidance literature:: Multi-step reaction with 2 steps

1: DCC / ethyl acetate / 2 h / 0 - 20 °C

2: DIEA / tetrahydrofuran

With N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jm9604078