N-Phenyl-D-xylosylamin

Base Information

Chemical Name:N-Phenyl-D-xylosylamin
CAS No.:58526-80-0
Molecular Formula:C₁₁H₁₅NO₄
Molecular Weight:225.244
Hs Code.:

Synonyms:N-Phenyl-D-xylosylamin

Suppliers and Price of N-Phenyl-D-xylosylamin

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-Phenyl-D-xylosylamin

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of N-Phenyl-D-xylosylamin

There total 9 articles about N-Phenyl-D-xylosylamin 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:

: 58-86-6
D-xylose

: 62-53-3
aniline

: 58526-80-0
N-Phenyl-D-xylosylamin

Guidance literature:: With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In water; at 22 ℃; for 2h;
DOI:10.1021/ac801693c

Reference yield:

: 2-O-benzyl-D-ribose

: 58526-80-0
D-ribose anilide

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / H₂ / 10percent Pd-C / ethanol / Ambient temperature

With hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1246/cl.1981.1005

Reference yield:

: 79241-01-3,79298-12-7,80572-05-0,119785-98-7
3,4-anhydro-5,6-dideoxy-1,2-O-isopropylidene-D-arabino-5-hexenitol

: 58526-80-0
D-ribose anilide

Guidance literature:: Multi-step reaction with 5 steps

1: 52 percent / neutral alumina / diethyl ether / Ambient temperature

2: 1.) ozone, 2.) dimethyl sulfide / 1.) dichloromethane, -78 deg C

3: silica gel

4: 91 percent / H₂ / 10percent Pd-C / ethanol / Ambient temperature

With aluminum oxide; dimethylsulfide; hydrogen; silica gel; ozone; palladium on activated charcoal; In diethyl ether; ethanol;
DOI:10.1246/cl.1981.1005