Fmoc-Met-OH

Modify Date: 2024-01-02 17:45:36

Fmoc-Met-OH Structure
Fmoc-Met-OH structure
Common Name Fmoc-Met-OH
CAS Number 71989-28-1 Molecular Weight 371.450
Density 1.3±0.1 g/cm3 Boiling Point 614.6±55.0 °C at 760 mmHg
Molecular Formula C20H21NO4S Melting Point 121-123 °C(lit.)
MSDS Chinese USA Flash Point 325.5±31.5 °C

 Use of Fmoc-Met-OH


Fmoc-Met-OH is a Methionine (HY-13694) derivative[1].

 Names

Name FMOC-L-Methionine
Synonym More Synonyms

 Fmoc-Met-OH Biological Activity

Description Fmoc-Met-OH is a Methionine (HY-13694) 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):1793-1144.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 614.6±55.0 °C at 760 mmHg
Melting Point 121-123 °C(lit.)
Molecular Formula C20H21NO4S
Molecular Weight 371.450
Flash Point 325.5±31.5 °C
Exact Mass 371.119141
PSA 100.93000
LogP 4.59
Vapour Pressure 0.0±1.9 mmHg at 25°C
Index of Refraction 1.616
Storage condition 2~8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090

 Synthetic Route

~98%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Di Gioia, Maria Luisa; Leggio, Antonella; Le Pera, Adolfo; Liguori, Angelo; Perri, Francesca; Siciliano, Carlo European Journal of Organic Chemistry, 2004 , # 21 p. 4437 - 4441

~85%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Ibrahim, Tarek S.; Tala, Srinivasa R.; El-Feky, Said A.; Abdel-Samii, Zakaria K.; Katritzky, Alan R. Synlett, 2011 , # 14 art. no. S03511ST, p. 2013 - 2016

~61%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Nowshuddin, Shaik; Rao; Reddy, A. Ram Synthetic Communications, 2009 , vol. 39, # 11 p. 2022 - 2031

~84%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Schoen, Istvan; Kisfaludy, Lajos Synthesis, 1986 , # 4 p. 303 - 305

~%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Synlett, , # 1 art. no. W17911ST, p. 142 - 144

~%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Organic Preparations and Procedures International, , vol. 30, # 2 p. 183 - 186

~%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Organic Preparations and Procedures International, , vol. 30, # 2 p. 183 - 186

~%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Synlett, , # 14 art. no. S03511ST, p. 2013 - 2016

~%

Fmoc-Met-OH Structure

Fmoc-Met-OH

CAS#:71989-28-1

Literature: Journal of the Chinese Chemical Society, , vol. 58, # 4 p. 509 - 515

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles2

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Synthesis, evaluation and molecular docking studies of amino acid derived N-glycoconjugates as antibacterial agents.

Bioorg. Chem. 63 , 110-5, (2015)

Six amino acid derived N-glycoconjugates of d-glucose were synthesized, characterized and tested for antibacterial activity against G(+)ve (Bacillus cereus) as well as G(-)ve (Escherichia coli and Kle...

Correlations of amyloid-β concentrations between CSF and plasma in acute Alzheimer mouse model.

Sci. Rep. 4 , 6777, (2014)

Amyloid-β (Aβ) is one of the few neuropathological biomarkers associated with transporters of the blood-brain barrier (BBB). Despite the well-characterized clinical indication of decreasing Aβ levels ...

 Synonyms

Fmoc-methionine
L-Methionine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
N-FMOC-L-MET
EINECS 276-258-5
MFCD00037134
Fmoc-Met-OH
FMOC-MET
N-[(9H-Fluoren-9-yl methoxy)carbonyl]-L-methionine
Fmoc-L-Met-OH
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-methionine
N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-methionine
Fmoc-Methionine-OH
N-FMOC-MET-OH
FMOC-L-MET
N-Fmoc-L-Met-OH
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