PHT-LEU-OH
Base Information
- Chemical Name: PHT-LEU-OH
- CAS No.: 2419-38-7
High Quality Chinese Factory supply 2419-38-7 PHT-LEU-OH
- Molecular Formula: C14H15NO4
- Molecular Weight: 261.277
- Vapor Pressure: 4.95E-08mmHg at 25°C
- Boiling Point: 426.4 °C at 760 mmHg
- Flash Point: 211.7 °C
- PSA： 74.68000
- Density: 1.311 g/cm3
- LogP: 1.71980
PHT-LEU-OH(Cas 2419-38-7) Usage
InChI:InChI=1/C14H15NO4/c1-8(2)7-11(14(18)19)15-12(16)9-5-3-4-6-10(9)13(15)17/h3-6,8,11H,7H2,1-2H3,(H,18,19)/p-1/t11-/m1/s1
2419-38-7 Relevant articles
Absolute configuration of α-phthalimido carboxylic acid derivatives from circular dichroism spectra
Skowronek,Gawronski
, p. 4585 - 4590 (1999)
It is demonstrated that the Cotton effec...
Enantiomerically Pure [2.2]Paracyclophane-4-thiol: A Planar Chiral Sulfur-Based Building Block Readily Available by Resolution with an Amino Acid Chiral Auxiliary
Vincent, Adrien,Deschamps, Damien,Martzel, Thomas,Lohier, Jean-Fran?ois,Richards, Christopher J.,Gaumont, Annie-Claude,Perrio, Stéphane
, p. 3961 - 3966 (2016)
Acyl chloride of N-phthaloyl-(S)-isoleuc...
Stereocontrolled synthesis of (S)-γ-fluoroleucine
Padmakshan, Dharshana,Bennett, Simon A.,Otting, Gottfried,Easton, Christopher J.
, p. 1083 - 1084 (2007)
Starting with (S)-leucine, the correspon...
Chiral sensors for determining the absolute configurations of α-amino acid derivatives
Chen, Zhongxiang,Fan, Hongjun,Yang, Shiwei,Bian, Guangling,Song, Ling
, p. 6933 - 6939 (2018)
A simple strategy for configurational as...
Structure-Activity Relationships for the Marine Natural Product Sintokamides: Androgen Receptor N-Terminus Antagonists of Interest for Treatment of Metastatic Castration-Resistant Prostate Cancer
Yan, Luping,Banuelos, Carmen A.,Mawji, Nasrin R.,Patrick, Brian O.,Sadar, Marianne D.,Andersen, Raymond J.
, p. 797 - 813 (2020/11/13)
Synthetic analogues of the marine natura...
Photoinduced and Palladium-Catalyzed Remote Desaturation of Amide Derivatives
Jin, Weiwei,Yu, Shouyun
supporting information, p. 6931 - 6935 (2021/09/11)
A photoinduced and palladium-catalyzed r...
DUAL KINASE-BROMODOMAIN INHIBITORS
-
Page/Page column 92; 123; 124, (2021/12/12)
Provided herein are compounds of Formula...
A base-controlled switch of SO2 reincorporation in photocatalyzed radical difunctionalization of alkenes
Bellotti, Peter,Glorius, Frank,Paulisch, Tiffany O.,Wang, Huamin,Zhang, Xiaolong
supporting information, p. 3412 - 3424 (2021/12/14)
Control of selectivity is a pivotal chal...
2419-38-7 Process route
-
-
6707-69-3
N-(o-carboxybenzoyl)-L-leucine
-
-
61-90-5,21675-61-6,25248-98-0,70-45-1
L-leucine
-
-
88-99-3,73607-73-5
benzene-1,2-dicarboxylic acid
-
-
2419-38-7
N-phthaloyl-(S)-leucine
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; potassium chloride;
In
acetonitrile;
at 50 ℃;
pH=1.00;
Further Variations:;
pH-values;
Kinetics;
Product distribution;
|
-
-
61-90-5,21675-61-6,25248-98-0,70-45-1
L-leucine
-
-
22509-74-6
N-ethoxycarbonylphthalimide
-
-
2419-38-7
N-phthaloyl-(S)-leucine
| Conditions | Yield |
|---|---|
|
With
sodium carbonate;
In
water;
at 20 ℃;
for 2h;
|
100%
|
|
With
sodium carbonate;
In
water;
at 20 ℃;
for 2h;
|
100%
|
|
With
sodium hydrogencarbonate;
In
water;
for 1h;
Ambient temperature;
|
66%
|
|
With
sodium carbonate;
In
water;
|
35%
|
|
With
sodium carbonate;
In
water;
at 20 ℃;
for 5h;
|
|
|
With
sodium carbonate;
In
water;
at 20 ℃;
for 3h;
|
2419-38-7 Upstream products
-
85-44-9
phthalic anhydride
-
61-90-5
L-leucine
-
5115-64-0
N -(1-carboxy-3-methyl-butyl)-phthalamic acid
-
22509-74-6
N-ethoxycarbonylphthalimide
2419-38-7 Downstream products
-
30816-20-7
N ,N -phthaloyl-L-leucine anilide
-
342392-03-4
N ,N -phthaloyl-L-leucine-[2]naphthylamide
-
19506-89-9
N-phthaloyl-DL-leucine
-
99036-46-1
N ,N -phthaloyl-L-leucine-(4-nitro-phenyl ester)
Product recommendations
- L-Serine methyl ester hydrochloride
- methyl 2,5-dimethyl-2-vinylhex-4-enoate
- 1-NITROANTHRAQUINONE
- Heptafluoropropyl trifluorovinyl ether
- 2'-Deoxycytidine hydrochloride
- Dioctyl(maleate)tin
- 1-ethyl-2-[1,2,3,4-tetrahydro-1-(2-hydroxyethyl)-2,2,4-trimethyl-6-quinolyl]benz[cd]indolium acetate
- 2,2'-[[3-[2-(dodecyloxy)ethoxy]propyl]imino]bisethanol