(S)-N-Boc-2-(5'-hexyl)glycine

Base Information

Chemical Name:(S)-N-Boc-2-(5'-hexyl)glycine
CAS No.:552335-71-4
Molecular Formula:C13H23NO4
Molecular Weight:257.33
Hs Code.:
Mol file:552335-71-4.mol

Synonyms:(S)-2-(tert-butoxycarbonylamino)oct-7-enoic acid;

Suppliers and Price of (S)-N-Boc-2-(5'-hexyl)glycine

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

Activate Scientific
(S)-2-(Boc-amino)oct-7-enoic acid 95% ee
1 g
$ 655.00

Acrotein
(S)-2-(Boc-amino)oct-7-enoicacid 97%
0.25g
$ 247.50

ACHEMBLOCK
(S)-2-(Boc-amino)oct-7-enoicacid 95%
250MG
$ 300.00

Total 5 raw suppliers

Chemical Property of (S)-N-Boc-2-(5'-hexyl)glycine

Chemical Property:

PSA：75.63000
LogP:3.10160

Purity/Quality:

97% (HPLC) ^*data from raw suppliers

(S)-2-(Boc-amino)oct-7-enoic acid 95% ee ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-N-Boc-2-(5'-hexyl)glycine

There total 16 articles about (S)-N-Boc-2-(5'-hexyl)glycine 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: 80.2%

: C₁₅H₂₈INO₄

: 552335-71-4
Boc-L-2-amino-7-octenoic acid

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 10 ℃; for 12h;

Reference yield:

: C₁₅H₂₇NO₄

: 552335-71-4
Boc-L-2-amino-7-octenoic acid

: C₁₅H₂₇NO₄

Guidance literature:: With ammonium hydroxide; water; subtilisin Carlsberg from Bacillus licheniformis; In N,N-dimethyl-formamide; at 38 ℃; for 4h; pH=7 - 8; Enzymatic reaction;
DOI:10.1016/j.bmc.2014.06.031

Reference yield:

: 947608-63-1
2(S)-tert-butoxycarbonylamino-oct-7-enoic acid ethyl ester

: 552335-71-4
Boc-L-2-amino-7-octenoic acid

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 0 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jacs.1c03903