N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Base Information

Chemical Name:N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid
CAS No.:99744-68-0
Molecular Formula:C₃₄H₄₄N₂O₅P*Cl
Molecular Weight:627.161
Hs Code.:

Synonyms:N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Suppliers and Price of N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

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

Total 0 raw suppliers

Chemical Property of N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

There total 5 articles about N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid 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: 94.0%

: 99744-56-6
N-<2-(Triphenylphosphonio)isopropyloxy>-L-leucyl-L-leucin-tert-butylester-chlorid

: 99744-68-0
N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Guidance literature:: With hydrogenchloride; In dichloromethane; at -70 ℃; for 0.5h;

Reference yield:

: 36466-73-6
(2-Hydroxypropyl)triphenylphosphonium-chlorid

: 99744-68-0
N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / CHCl₃ / 5 h / -15 °C

2: CHCl₃ / 12 h / Ambient temperature

3: 90 percent / EEDQ / CHCl₃ / 15 h / Ambient temperature

4: 94 percent / HCl / CH₂Cl₂ / 0.5 h / -70 °C

With hydrogenchloride; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane; chloroform;

Reference yield:

: 99744-31-7
<2-(Chlorformyl)-2-methylethyl>triphenylphosphonium-chlorid

: 99744-68-0
N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-leucyl-L-leucin-chlorid

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 12 h / Ambient temperature

2: 90 percent / EEDQ / CHCl₃ / 15 h / Ambient temperature

3: 94 percent / HCl / CH₂Cl₂ / 0.5 h / -70 °C

With hydrogenchloride; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane; chloroform;