94744-50-0
- Product Name：Fmoc-Aib-OH
- Molecular Formula：C19H19NO4
- Purity：99%
- Molecular Weight：325.364
Product Details;
CAS#： 94744-50-0
Molecular Formula： C19H19NO4
Chinese Factory Supply 94744-50-0 with Efficient Transportation, Buy Quality Fmoc-Aib-OH
- Molecular Formula:C19H19NO4
- Molecular Weight:325.364
- Melting Point:182-188 °C
- Refractive Index:1.614
- Boiling Point:544.3 °C at 760 mmHg
- PKA:3.98±0.10(Predicted)
- Flash Point:283 °C
- PSA：75.63000
- Density:1.256 g/cm3
- LogP:3.77920
Fmoc-Aib-OH(Cas 94744-50-0) Usage
InChI:InChI=1/C19H19NO4/c1-19(20,18(22)23)10-17(21)24-11-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,16H,10-11,20H2,1H3,(H,22,23)
94744-50-0 Relevant articles
Radical-Mediated Activation of Esters with a Copper/Selectfluor System: Synthesis of Bulky Amides and Peptides
Matsumoto, Akira,Wang, Zhe,Maruoka, Keiji
, p. 5401 - 5411 (2021/04/12)
Herein, we describe a new approach for t...
GLP-1 PRODRUGS
-
Page/Page column, (2015/02/25)
The invention relates to a GLP-1 prodrug...
A one-pot procedure for the preparation of N-9-fluorenylmethyloxycarbonyl- α-amino diazoketones from α-amino acids
Siciliano, Carlo,De Marco, Rosaria,Guidi, Ludovica Evelin,Spinella, Mariagiovanna,Liguori, Angelo
, p. 10575 - 10582 (2013/02/22)
The study describes a new "one-pot" rout...
Exploiting an inherent neighboring group effect of α-amino acids to synthesize extremely hindered dipeptides
Brown, Zachary Z.,Schafmeister, Christian E.
supporting information; experimental part, p. 14382 - 14383 (2009/02/08)
The creation of highly hindered peptides...
94744-50-0 Process route
-
- 28920-43-6
(fluorenylmethoxy)carbonyl chloride
-
- 5938-34-1
2-amino-2-methyl-propanoic acid hydrochloride
-
![N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid](/upload/2024/7/b99e481f-aaef-4f14-8899-7f47ff73cfb5.png)
- 94744-50-0
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid
| Conditions | Yield |
|---|---|
|
With water; sodium carbonate; In 1,4-dioxane; for 16h;
|
83% |
|
With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 20 ℃; for 2h;
|
-
-
2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-propionic acid tert-butyl ester
-
- 94744-50-0
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid
| Conditions | Yield |
|---|---|
|
With ytterbium(III) triflate; In nitromethane; at 45 - 50 ℃; for 5h;
|
97% |
94744-50-0 Upstream products
-
28920-43-6
(fluorenylmethoxy)carbonyl chloride
-
5938-34-1
2-amino-2-methyl-propanoic acid hydrochloride
-
62-57-7
2-Aminoisobutyric acid
-
920-66-1
1,1,1,3',3',3'-hexafluoro-propanol
94744-50-0 Downstream products
-
145645-77-8
trans-2-Fluorenyl-methoxycarbonylamino-2-methyl-N-(4-nitroxycyclohexyl)-propionsaeureamid
-
150458-43-8
Fmoc-Aib-SA
-
186096-83-3
(S)-1-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-2-methyl-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester
-
186096-86-6
(S)-1-[2-({(2S,4R)-4-tert-Butoxy-1-[2-(9H-fluoren-9-ylmethoxycarbonylamino)-2-methyl-propionyl]-pyrrolidine-2-carbonyl}-amino)-2-methyl-propionyl]-pyrrolidine-2-carboxylic acid tert-butyl ester
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