(S)-2-N-Cbz-Amino-pentane-1,5-diol

Base Information

Chemical Name:(S)-2-N-Cbz-Amino-pentane-1,5-diol
CAS No.:478646-26-3
Molecular Formula:C13H19NO4
Molecular Weight:253.298
Hs Code.:2924299090
DSSTox Substance ID:DTXSID30427448
Wikidata:Q82240109
Mol file:478646-26-3.mol

Synonyms:(S)-2-N-Cbz-Amino-pentane-1,5-diol;478646-26-3;benzyl N-[(2S)-1,5-dihydroxypentan-2-yl]carbamate;(s)-2-n-cbz-aminopentane-1,5-diol;(S)-benzyl 1,5-dihydroxypentan-2-ylcarbamate;(S)-Benzyl (1,5-dihydroxypentan-2-yl)carbamate;SCHEMBL1571205;DTXSID30427448;MFCD03426375;benzyl (s)-1,5-dihydroxypentan-2-ylcarbamate;(S)-Benzyl(1,5-dihydroxypentan-2-yl)carbamate;EN300-12612452

Suppliers and Price of (S)-2-N-Cbz-Amino-pentane-1,5-diol

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
(S)-Benzyl(1,5-dihydroxypentan-2-yl)carbamate 97%
25g
$ 414.00

American Custom Chemicals Corporation
(S)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL 95.00%
10G
$ 1359.50

Total 11 raw suppliers

Chemical Property of (S)-2-N-Cbz-Amino-pentane-1,5-diol

Chemical Property:

Vapor Pressure:3.17E-10mmHg at 25°C
Melting Point:103-105 °C
Boiling Point:485.2oC at 760 mmHg
PKA:11.77±0.46(Predicted)
Flash Point:247.2oC
PSA：78.79000
Density:1.192g/cm3
LogP:1.43710
XLogP3:0.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:8
Exact Mass:253.13140809
Heavy Atom Count:18
Complexity:229

Purity/Quality:

97% ^*data from raw suppliers

(S)-Benzyl(1,5-dihydroxypentan-2-yl)carbamate 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC(=O)NC(CCCO)CO
Isomeric SMILES:C1=CC=C(C=C1)COC(=O)N[C@@H](CCCO)CO

Technology Process of (S)-2-N-Cbz-Amino-pentane-1,5-diol

There total 2 articles about (S)-2-N-Cbz-Amino-pentane-1,5-diol 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: 79.0%

: 67436-17-3
dimethyl (S)-N-(benzyloxycarbonyl)glutamate

: 478646-26-3
(2S)-benzyl 1,5-dihydroxypentan-2-ylcarbamate

Guidance literature:: With lithium borohydride; In tetrahydrofuran; methanol; at 0 ℃; for 4h;
DOI:10.3987/COM-04-S(P)40

Reference yield:

: 1155-62-0
N-benzyloxycarbonyl-L-glutamic acid

: 478646-26-3
(2S)-benzyl 1,5-dihydroxypentan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / BF₃*OEt₂

2: 79 percent / LiBH₄ / methanol; tetrahydrofuran / 4 h / 0 °C

With lithium borohydride; boron trifluoride diethyl etherate; In tetrahydrofuran; methanol;
DOI:10.1002/ejoc.200400709