(S)-N-Boc-L-homoserine Triethylammonium Salt

Base Information

Chemical Name:(S)-N-Boc-L-homoserine Triethylammonium Salt
CAS No.:796072-25-8
Molecular Formula:C₆H₁₅N*C₉H₁₇NO₅
Molecular Weight:320.429
Hs Code.:
Mol file:796072-25-8.mol

Synonyms:(S)-2-(tert-Butoxycarbonylamino)-4-hydroxybutanoic Acid Triethylammonium Salt;(S)-N-Boc-L-homoserine Triethylammonium Salt;N-[(1,1-Dimethylethoxy)carbonyl]-L-homoserine Triethylammonium Salt;N-tert-Butoxycarbonyl-L-homoserine Triethylammonium Salt

Suppliers and Price of (S)-N-Boc-L-homoserine Triethylammonium Salt

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
(S)-N-Boc-L-homoserineTriethylammoniumSalt
100mg
$ 65.00

Biosynth Carbosynth
(S)-N-Boc-L-homoserine triethylammonium salt
250 mg
$ 182.50

Biosynth Carbosynth
(S)-N-Boc-L-homoserine triethylammonium salt
100 mg
$ 100.00

Biosynth Carbosynth
(S)-N-Boc-L-homoserine triethylammonium salt
1 g
$ 600.60

Biosynth Carbosynth
(S)-N-Boc-L-homoserine triethylammonium salt
500 mg
$ 335.00

AK Scientific
(S)-N-Boc-L-homoserineTriethylammoniumSalt
100mg
$ 185.00

Total 3 raw suppliers

Chemical Property of (S)-N-Boc-L-homoserine Triethylammonium Salt

Chemical Property:

PSA：102.59000
LogP:1.89920
Storage Temp.:-20°C Freezer
Solubility.:Water

Purity/Quality:

98% ^*data from raw suppliers

(S)-N-Boc-L-homoserineTriethylammoniumSalt ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (S)-N-Boc-L-homoserine Triethylammonium Salt

There total 2 articles about (S)-N-Boc-L-homoserine Triethylammonium Salt 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:

: 672-15-1,119736-88-8
L-homoserine

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

: 796072-25-8
(L)-N-tert-butoxycarbonylhomoserine triethylamine salt

Guidance literature:: With triethylamine; In water; acetone; at 0 ℃; for 16h;

Reference yield:

: 672-15-1,119736-88-8
L-homoserine

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

: 121-44-8
triethylamine

: 796072-25-8
(L)-N-tert-butoxycarbonylhomoserine triethylamine salt

Guidance literature:: In water; acetone; at 0 ℃; for 16h;

Reference yield:

: 796072-25-8
(L)-N-tert-butoxycarbonylhomoserine triethylamine salt

: 2-tert-butoxycarbonylamino-4-(4'-dibenzofuran-4-yl-biphenyl-4-ylsulfanyl)-butyric acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: DMF (N,N-dimethyl-formamide) / 16 h

2: carbon tetrabromide; triphenylphosphine / dichloromethane / 16 h / 20 °C

3: caesium carbonate / DMF (N,N-dimethyl-formamide) / 2 h / 0 - 20 °C

4: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / ethanol; water; toluene / 2 h / Heating / reflux

With carbon tetrabromide; potassium carbonate; caesium carbonate; triphenylphosphine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In DMF (N,N-dimethyl-formamide); ethanol; dichloromethane; water; toluene; 4: Suzuki Coupling;