Z-L-DAP(BOC)-OBN

Base Information

Chemical Name:Z-L-DAP(BOC)-OBN
CAS No.:239785-37-6
Molecular Formula:C23H28N2O6
Molecular Weight:428.48
Hs Code.:
Mol file:239785-37-6.mol

Synonyms:Z-L-DAP(BOC)-OBN;3-[[(1,1-DiMethylethoxy)carbonyl]aMino]-N-[(phenylMethoxy)carbonyl]-;3-(Boc-amino)-N-Cbz-L-alanine phenylmethyl ester

Suppliers and Price of Z-L-DAP(BOC)-OBN

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
Z-L-Dap(Boc)-Obn
1g
$ 1055.00

Biosynth Carbosynth
Z-L-Dap(boc)-obn
1 g
$ 1310.40

Biosynth Carbosynth
Z-L-Dap(boc)-obn
100 mg
$ 219.00

Biosynth Carbosynth
Z-L-Dap(boc)-obn
50 mg
$ 120.50

Biosynth Carbosynth
Z-L-Dap(boc)-obn
500 mg
$ 720.00

Biosynth Carbosynth
Z-L-Dap(boc)-obn
250 mg
$ 397.50

American Custom Chemicals Corporation
Z-L-DAP(BOC)-OBN 95.00%
1G
$ 311.54

Activate Scientific
3-(Boc-amino)-N-Cbz-L-alanine phenylmethyl ester 95+%
1 g
$ 336.00

Activate Scientific
3-(Boc-amino)-N-Cbz-L-alanine phenylmethyl ester 95+%
5 g
$ 858.00

Acrotein
3-(Boc-amino)-N-Cbz-L-alaninephenylmethylester 97%
10g
$ 1008.33

Total 5 raw suppliers

Chemical Property of Z-L-DAP(BOC)-OBN

Chemical Property:

Boiling Point:598.6±50.0 °C(Predicted)
PKA:10.61±0.46(Predicted)
PSA：109.94000
Density:1.190±0.06 g/cm3(Predicted)
LogP:3.95830

Purity/Quality:

99% ^*data from raw suppliers

Z-L-Dap(Boc)-Obn ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Z-L-DAP(BOC)-OBN is used in the preparation of N-hydroxybenzamidine derivatives of β-amino-L-alanine with potent affinity to receptor of cell adhesion activating protein. Used in the preparation of N-hydroxybenzamidine derivatives of β-amino-L-alanine with potent affinity to receptor of cell adhesion activating protein.

Technology Process of Z-L-DAP(BOC)-OBN

There total 2 articles about Z-L-DAP(BOC)-OBN 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:

: 16947-84-5,62234-36-0
N-[(benzyloxy)carbonyl]-3-[(tert-butoxycarbonyl)amino]-L-alanine

: 100-39-0
benzyl bromide

: 239785-37-6
benzyl (S)-2-(((benzyloxy)carbonyl)amino)-3-((tert-butoxycarbonyl)amino)propanoate

Guidance literature:: With sodium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 3h;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 35761-26-3
(S)-3-amino-2-(((benzyloxy)carbonyl)amino)propanoic acid

: 239785-37-6
benzyl (S)-2-(((benzyloxy)carbonyl)amino)-3-((tert-butoxycarbonyl)amino)propanoate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate / water; tetrahydrofuran / 3 h / 20 °C

2: sodium carbonate / N,N-dimethyl-formamide / 3 h / 20 °C

With sodium carbonate; In tetrahydrofuran; water; N,N-dimethyl-formamide;