Boc-Phe-Ala-OH

Modify Date: 2024-01-06 18:23:34

Boc-Phe-Ala-OH Structure
Boc-Phe-Ala-OH structure
Common Name Boc-Phe-Ala-OH
CAS Number 55677-48-0 Molecular Weight 336.38300
Density 1.182g/cm3 Boiling Point 587.8ºC at 760mmHg
Molecular Formula C17H24N2O5 Melting Point 90-93℃
MSDS N/A Flash Point 309.3ºC

 Use of Boc-Phe-Ala-OH


(tert-Butoxycarbonyl)-L-phenylalanyl-L-alanine is an alanine derivative[1].

 Names

Name (2S)-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]propanoic acid
Synonym More Synonyms

 Boc-Phe-Ala-OH Biological Activity

Description (tert-Butoxycarbonyl)-L-phenylalanyl-L-alanine is an alanine derivative[1].
Related Catalog
In Vitro Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].
References

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1083.

 Chemical & Physical Properties

Density 1.182g/cm3
Boiling Point 587.8ºC at 760mmHg
Melting Point 90-93℃
Molecular Formula C17H24N2O5
Molecular Weight 336.38300
Flash Point 309.3ºC
Exact Mass 336.16900
PSA 104.73000
LogP 2.49350
Index of Refraction 1.53
Storage condition 2-8℃

 Synthetic Route

~78%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Fustero, Santos; Sancho, Amador Garcia; Chiva, Gema; Sanz-Cervera, Juan F.; Del Pozo, Carlos; Acena, Jose Luis Journal of Organic Chemistry, 2006 , vol. 71, # 8 p. 3299 - 3302

~95%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Katritzky, Alan R.; Suzuki, Kazuyuki; Singh, Sandeep K. Synthesis, 2004 , # 16 p. 2645 - 2652

~83%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Popovic, Stanimir; Bieraeugel, Hans; Detz, Remko J.; Kluwer, Alexander M.; Koole, Jelmer A. A.; Streefkerk, Dieuwertje E.; Hiemstra, Henk; Van Maarseveen, Jan H. Chemistry - A European Journal, 2013 , vol. 19, # 50 p. 16934 - 16937

~86%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Martinez, Jean; Laur, Janine; Castro, Bertrand Tetrahedron, 1985 , vol. 41, # 4 p. 739 - 744

~%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Gewehr, Markus; Kunz, Horst Synthesis, 1997 , # 12 p. 1499 - 1510

~%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Verardo; Gorassini Journal of Peptide Science, 2013 , vol. 19, # 5 p. 315 - 324

~%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Zajdlik, Adam; Wang, Zezhou; Hickey, Jennifer L.; Aman, Ahmed; Schimmer, Aaron D.; Yudin, Andrei K. Angewandte Chemie - International Edition, 2013 , vol. 52, # 32 p. 8411 - 8415 Angew. Chem., 2013 , vol. 125, # 32 p. 8569 - 8573

~%

Boc-Phe-Ala-OH Structure

Boc-Phe-Ala-OH

CAS#:55677-48-0

Literature: Chen, Shui-Tein; Chang, Chung-Ho; Wang, Kung-Tsung Journal of Chemical Research, Miniprint, 1991 , # 8 p. 1967 - 1975

 Synonyms

t-Butyloxycarbonylphenylalanylalanine
Boc-phenylalanyl-alanine
t-butyloxycarbonyl-L-phenylalanyl-L-alanine
Boc-phe-ala
BOC-L-PHENYLALANYL ALANINE
N-tert-butyloxycarbonyl-L-phenylalanyl-L-alanine
Boc-Phe-Ala-OH
N-Boc-PheAla