Boc-D-isoleucine

Base Information

Chemical Name:Boc-D-isoleucine
CAS No.:55721-65-8
Molecular Formula:C11H21NO4
Molecular Weight:231.292
Hs Code.:29224999
Mol file:55721-65-8.mol

Synonyms:N-tert-Butoxycarbonyl-D-isoleucine;

Suppliers and Price of Boc-D-isoleucine

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-L-Ile-OH
100g
$ 376.00

TRC
N-Boc-D-isoleucine
500mg
$ 1375.00

TRC
N-Boc-D-isoleucine
50mg
$ 165.00

TRC
N-Boc-D-isoleucine
250mg
$ 745.00

Sigma-Aldrich
Boc-D-Ile-OH ≥98.0% (TLC)
1g
$ 353.00

Crysdot
Boc-D-Ile-OH 95+%
5g
$ 450.00

ChemPep
Boc-D-Ile-OH?1/2H2O ≥98%
5g
$ 650.00

Chem-Impex
Boc-D-isoleucine ≥ 99% (HPLC)
5G
$ 745.00

Chem-Impex
Boc-D-isoleucine ≥ 99% (HPLC)
250MG
$ 90.00

Chem-Impex
Boc-D-isoleucine,≥99%(HPLC) ≥99%(HPLC)
1G
$ 209.66

Total 45 raw suppliers

Chemical Property of Boc-D-isoleucine

Chemical Property:

Melting Point:63-65 °C
Refractive Index:1.461
Boiling Point:356.041 °C at 760 mmHg
PKA:4.03±0.22(Predicted)
Flash Point:169.128 °C
PSA：75.63000
Density:1.062 g/cm³
LogP:2.40130
Storage Temp.:−20°C

Purity/Quality:

99% ^*data from raw suppliers

Boc-L-Ile-OH ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses N-Boc-D-isoleucine is an N-Boc-protected form of D-Isoleucine (I820210). D-Isoleucine is not biosynthesized in the human body and is therefore categorized as an essential amino acid that must be obtained through diet. It is also an important building block that is used in the formation of hemoglobin in humans.

Technology Process of Boc-D-isoleucine

There total 37 articles about Boc-D-isoleucine 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: 99.0%

: 1509-34-8,959215-79-3,18875-42-8
D-allo-isoleucine

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

: 13139-16-7,35264-07-4,55721-65-8,55780-90-0,116194-21-9
Boc-L-aIle-OH

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; for 2h; 0 deg C to r. t.;
DOI:10.1021/jo00037a012

Reference yield: 96.0%

: 1509-35-9,959215-79-3,18875-42-8
D-alloisoleucine

: 2-((tert-butoxycarbonyloxy)imino)-2-phenylacetonitrile

: 13139-16-7,35264-07-4,55721-65-8,55780-90-0,116194-21-9
N-tert-butoxycarbonyl-D-alloisoleucine

Guidance literature:: With triethylamine; In water; acetone; for 5h; Ambient temperature;
DOI:10.1021/jo00037a012

Reference yield:

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

: 959215-79-3,18875-42-8
(2RS,3S)-2-amino-3-methylpentanoic acid

: 13139-16-7
N-(tert-butyloxycarbonyl)-L-isoleucine

: 13139-16-7,35264-07-4,55721-65-8,55780-90-0,116194-21-9
N-tert-butoxycarbonyl-D-alloisoleucine

Guidance literature:: With sodium hydroxide; In 1,4-dioxane; water; at 0 - 22 ℃; pH=9 - 10; Overall yield = 88 %; Overall yield = 0.77 g; diastereoselective reaction;
DOI:10.1039/c5ob02520f