BOC-D-HSE(BZL)-OH

Base Information

Chemical Name:BOC-D-HSE(BZL)-OH
CAS No.:150009-60-2
Molecular Formula:C₁₆H₂₃NO₅
Molecular Weight:309.362
Hs Code.:
Mol file:150009-60-2.mol

Synonyms:(2R)-4-benzyloxy-2-(tert-butoxycarbonylamino)butanoic acid;O-benzyl-N-(tert-butoxycarbonyl)-D-homoserine;(2R)-4-(Benzyl-Oxy)-2-{[(Tert-Butoxy)Carbonyl]Amino}Butanoic Acid;

Suppliers and Price of BOC-D-HSE(BZL)-OH

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

Usbiological
Boc-O-benzyl-D-homoserine
1g
$ 379.00

TRC
Boc-d-hse(bzl)-oh
1g
$ 220.00

TRC
Boc-d-hse(bzl)-oh
500mg
$ 155.00

Iris Biotech GmbH
Boc-D-Hse(Bzl)-OH
25 g
$ 1350.00

Iris Biotech GmbH
Boc-D-Hse(Bzl)-OH
1 g
$ 114.75

Iris Biotech GmbH
Boc-D-Hse(Bzl)-OH
5 g
$ 378.00

Crysdot
(R)-4-(Benzyloxy)-2-((tert-butoxycarbonyl)amino)butanoicacid 95+%
5g
$ 470.00

Crysdot
(R)-4-(Benzyloxy)-2-((tert-butoxycarbonyl)amino)butanoicacid 95+%
1g
$ 158.00

Chem-Impex
Boc-O-benzyl-D-homoserine,99%(HPLC) 99%(HPLC)
250MG
$ 44.80

Chem-Impex
Boc-O-benzyl-D-homoserine,99%(HPLC) 99%(HPLC)
1G
$ 134.40

Total 15 raw suppliers

Chemical Property of BOC-D-HSE(BZL)-OH

Chemical Property:

Vapor Pressure:4.82E-10mmHg at 25°C
Refractive Index:1.519
Boiling Point:480.5 °C at 760 mmHg
PKA:3.83±0.10(Predicted)
Flash Point:244.4 °C
PSA：84.86000
Density:1.154 g/cm³
LogP:2.96210
Storage Temp.:Store at 0-5°C

Purity/Quality:

98% ^*data from raw suppliers

Boc-O-benzyl-D-homoserine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of BOC-D-HSE(BZL)-OH

There total 6 articles about BOC-D-HSE(BZL)-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: 96.0%

: 4-benzyloxy-(2S)-tert-butoxycarbonylaminobutanoic acid benzyl ester

: 59408-74-1,150009-60-2
(S)-2-((tert-butoxy)carbonylamino)-4-(phenylmethoxy)butyric acid

Guidance literature:: With ammonium acetate; hydrogen; palladium on activated charcoal; In methanol; for 20h; Ambient temperature;
DOI:10.1016/0040-4039(95)00527-J

Reference yield: 89.12%

: 38308-92-8
2-(tert-butoxycarbonylamino)-4-hydroxy-butanoic acid

: 100-39-0
benzyl bromide

: 876617-13-9,150009-60-2
L-2-(tert-Butoxycarbonylamino)-4-(benzyloxy)butanoic acid

Guidance literature:: With triethylamine; In acetone; at 55 ℃; for 6h;

Reference yield:

: 1070-19-5
N-(tert-butyloxycarbonyl) azide

: 59408-74-1,150009-60-2
(S)-2-((tert-butoxy)carbonylamino)-4-(phenylmethoxy)butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: MgO / H₂O; dioxane

2: (i) Na, liq. NH₃, (ii) /BRN= 385801/

With magnesium oxide; In 1,4-dioxane; water;