Boc-DL-Phe-OH

Modify Date: 2024-01-02 19:21:13

Boc-DL-Phe-OH Structure
Boc-DL-Phe-OH structure
 Common Name Boc-DL-Phe-OH
CAS Number 4530-18-1 Molecular Weight 265.305
Density 1.2±0.1 g/cm3 Boiling Point 426.6±38.0 °C at 760 mmHg
Molecular Formula C14H19NO4 Melting Point N/A
MSDS USA Flash Point 211.8±26.8 °C

 Use of Boc-DL-Phe-OH


2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid is a phenylalanine derivative[1].

 Names

Name Boc-DL-Phenylalanine
Synonym More Synonyms

 Boc-DL-Phe-OH Biological Activity

Description 2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid is a phenylalanine 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):1793-882.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 426.6±38.0 °C at 760 mmHg
Molecular Formula C14H19NO4
Molecular Weight 265.305
Flash Point 211.8±26.8 °C
Exact Mass 265.131409
PSA 75.63000
LogP 2.96
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.528
Storage condition Store at RT.

 Safety Information

Hazard Codes Xi
Risk Phrases 43
Safety Phrases 36/37
HS Code 2924299090

 Synthetic Route

DL-Phenylalanine structure

DL-Phenylalanine

CAS#:150-30-1
Di-tert-butyl dicarbonate structure

Di-tert-butyl d...

CAS#:24424-99-5

~99%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: Caplar, Vesna; Zinic, Mladen; Pozzo, Jean-Luc; Fages, Frederic; Mieden-Gundert, Gudrun; Voegtle, Fritz European Journal of Organic Chemistry, 2004 , # 19 p. 4048 - 4059
N/A structure

N/A

CAS#:909114-65-4
DL-Phenylalanine structure

DL-Phenylalanine

CAS#:150-30-1

~86%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: Hioki, Kazuhito; Kinugasa, Mizuho; Kishimoto, Michiko; Fujiwara, Miho; Tani, Shohei; Kunishima, Munetaka Synthesis, 2006 , # 12 p. 1931 - 1933
DL-Phenylalanine structure

DL-Phenylalanine

CAS#:150-30-1
Carbonic acid, 1H-benzotriazol-1-yl 1,1-dimethylethyl ester structure

Carbonic acid, ...

CAS#:89037-64-9

~86%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: Kim, Sunggak; Chang, Heung Journal of the Chemical Society, Chemical Communications, 1983 , # 22 p. 1357 - 1358
DL-Phenylalanine structure

DL-Phenylalanine

CAS#:150-30-1
T-BUTYL-P-NITROPHENYL CARBONATE structure

T-BUTYL-P-NITRO...

CAS#:13303-10-1

~%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: Anderson; McGregor Journal of the American Chemical Society, 1957 , vol. 79, p. 6180,6181
Tris(4-bromophenyl)amine structure

Tris(4-bromophe...

CAS#:4316-58-9
N/A structure

N/A

CAS#:126686-59-7

~88%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: Dapperheld, Steffen; Steckhan, Eberhard Angewandte Chemie, 1982 , vol. 94, # 10 p. 785
Boc-Gly-OH structure

Boc-Gly-OH

CAS#:4530-20-5
Benzyl bromide structure

Benzyl bromide

CAS#:100-39-0

~%

Boc-DL-Phe-OH Structure

Boc-DL-Phe-OH

CAS#:4530-18-1
Literature: De Nicola; Einhorn; Luche Tetrahedron Letters, 1992 , vol. 33, # 43 p. 6461 - 6464

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Synonyms

boc-dl-phe-oh
N-tert-Butyloxycarbonyl-L-phenylalanine
Boc-phenylalanine
N-{[(2-Methyl-2-propanyl)oxy]carbonyl}-L-phenylalanine
(2S)-2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-phenylpropanoic acid
N-(tert-Butoxycarbonyl)-L-phenylalanin
N-(tert-Butoxycarbonyl)-L-phenylalanine
boc-L-Phe
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-
N-t-Butyloxycarbonyl-L-phenylalanine
L-Phenylalanine, N-((1,1-dimethylethoxy)carbonyl)-
N-α-t-BOC-L-phenylalanine
N-Boc-L-phenylalanine
MFCD00153311
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