Z-D-homoserine lactone

Base Information

Chemical Name:Z-D-homoserine lactone
CAS No.:41088-89-5
Molecular Formula:C12H13NO4
Molecular Weight:235.24
Hs Code.:
Mol file:41088-89-5.mol

Synonyms:Carbamicacid, (tetrahydro-2-oxo-3-furanyl)-, phenylmethyl ester, (R)-;

Suppliers and Price of Z-D-homoserine lactone

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

Crysdot
(R)-Benzyl(2-oxotetrahydrofuran-3-yl)carbamate 95+%
5g
$ 475.00

Chemenu
benzyl(R)-(2-oxotetrahydrofuran-3-yl)carbamate 95%
5g
$ 444.00

Biosynth Carbosynth
Cbz-D-homoserinelactone
25 mg
$ 405.00

Biosynth Carbosynth
Cbz-D-homoserinelactone
5 mg
$ 117.00

Biosynth Carbosynth
Cbz-D-homoserinelactone
2 mg
$ 59.00

Biosynth Carbosynth
Cbz-D-homoserinelactone
10 mg
$ 203.00

Biosynth Carbosynth
Cbz-D-homoserinelactone
50 mg
$ 704.00

American Custom Chemicals Corporation
CBZ-D-HOMOSERINE LACTONE 95.00%
250MG
$ 646.00

American Custom Chemicals Corporation
CBZ-D-HOMOSERINE LACTONE 95.00%
5MG
$ 502.66

Ambeed
(R)-Benzyl(2-oxotetrahydrofuran-3-yl)carbamate 98+%
5g
$ 139.00

Total 40 raw suppliers

Chemical Property of Z-D-homoserine lactone

Chemical Property:

Boiling Point:466.1 °C at 760 mmHg
PKA:11.00±0.20(Predicted)
Flash Point:235.7 °C
Density:1.272 g/cm³
Storage Temp.:2-8°C

Purity/Quality:

99% ^*data from raw suppliers

(R)-Benzyl(2-oxotetrahydrofuran-3-yl)carbamate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Z-D-homoserine lactone

There total 7 articles about Z-D-homoserine lactone 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: 74.0%

: 6027-21-0,119736-88-8
D-homoserine

: 501-53-1,94274-21-2
benzyl chloroformate

: 41088-89-5
D-2-<(benzyloxycarbonyl)amino>-4-butyrolactone

Guidance literature:: D-homoserine; benzyl chloroformate; With sodium hydrogencarbonate; In water; at 0 - 20 ℃; for 18.5h; Inert atmosphere;

With hydrogenchloride; In water; pH=2; Inert atmosphere;
DOI:10.1021/jm2004305

Reference yield: 20.0%

: 1152-62-1,4434-61-1,28862-80-8
(2R)-2-[[(benzyloxy)carbonyl]amino]-4-(methylsulfanyl)butanoic acid

: 41088-89-5
D-2-<(benzyloxycarbonyl)amino>-4-butyrolactone

Guidance literature:: With hydrogen fluoride; methyl iodide; In acetic acid; for 15h;
DOI:10.1139/v03-122

Reference yield:

: 6027-21-0,119736-88-8
D-homoserine

: 501-53-1,94274-21-2
benzyl chloroformate

: 41088-85-1
N-[(phenylmethoxy)carbonyl]-D-homoserine

: 41088-89-5
D-2-<(benzyloxycarbonyl)amino>-4-butyrolactone

Guidance literature:: With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 1h; Title compound not separated from byproducts.;
DOI:10.1021/ol990148r