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86069-86-5

86069-86-5 structure
86069-86-5 structure

Name Fmoc-(S)-(-)-piperidine-2-carboxylic acid
Synonyms (S)-N-FLUORENYLMETHOXYCBONYL-2-PIPERIDINECBOXYLIC ACID
(S)-1,2-Piperidinedicboxylic acid 1-(9H-fluoren-9-ylmethyl) ester
MFCD00235898
FMOC-L-PIPERIDINE-2-CBOXYLIC ACID
(S)-Piperidine-2-cboxylic acid, N-FMOC protected
L-1-N-FMOC-PIPECOLINIC ACID
(S)-1-Fmoc-piperidine-2-cboxylic acid, N-Fmoc-L-pipecolinic acid
(2S)-1-[9H-fluoren-9-ylmethoxy(oxo)methyl]-2-piperidinecboxylic acid
FMOC-PIPERIDINE-2-CBOXYLIC ACID
(S)-1-FMOC-PIPERIDINE-2-CBOXYLIC ACID
(S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecboxylic Acid
(9H-Fluoren-9-yl)MethOxy]carbonyl HoPro-OH
FMOC-B-HOMO-PRO-OH
N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-PIPECOLIC ACID
FMOC-L-(-)-PIPECOLIC ACID
N-FMoc-(S)-2-piperidinecboxylic acid
1-Fmoc-L-pipecolic Acid
(S)-1-FMOC-PIPERIDINE-2-CARBOXYLIC ACID
Fmoc-HoPro-OH
N-FMOC-(S)-PIPECOLINIC ACID
Fmo-L-homoproline (HPLC)
1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-pipecolic Acid
FMOC-HOPRO-OH
N-FMOC-L-PIPECOLINIC ACID
S)-PIPERIDINE-1
2,2-Piperidinedicarboxylic acid, 2-(9H-fluoren-9-ylmethyl) ester
(L)-N-FMOC-PIPECOLIC ACID
(S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecboxylicAcid>
2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid
FMOC-HOMOPROLINE
N-Fmoc-(2S)-piperidinecboxylic acid
(S)-N-(9-FLUORENYLMETHYLOXYCBONYL)-PIPERIDINE-2-CBOXYLIC ACID
fmoc-l-pipecolic acid
(S)-N-Fmoc-piperidine-2-cboxyL
FMOC-L-PIP-OH
(L)-N-(9-FLUORENYLMETHYLOXYCBONYL)PIPECOLIC ACID
(2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2-piperidinecarboxylic acid
FMO-L-HOMOPROLINE
Fmoc-HomoPro-OH
(S)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-cboxylic acid
N-ALPHA-(9-FLUORENYLMETHOXYCBONYL)-L-HOMOPROLINE
(S)-PIPERIDINE-1,2-DICBOXYLIC ACID 1-(9H-FLUOREN-9-YLMETHYL) ESTER
Fmoc-Pip-OH,(S)-1-Fmoc-piperidine-2-cboxylic acid, N-Fmoc-L-pipecolinic acid
(2S)-1-(9H-fluoren-9-ylmethoxycbonyl)piperidine-2-cboxylic acid
L-Pipecolinic acid, N-FMOC protected
(S)-N-Fmoc-piperidine-2-cboxylic acid
RECHEM BK PT 0274
FMOC-(S)-(-)-PIPERIDINE-2-CBOXYLIC ACID
N-ALPHA-FMOC-L-PIPECOLIC ACID
Fmoc-β-Homo-Pro-OH
(2S)-1-[(9H-Fluoren-9-ylmethoxy)carbonyl]piperidine-2-carboxylic acid
(S)-1-Fmoc-2-piperidinecboxylic Acid
FMOC-PIC(2)-OH
1,2-Piperidinedicboxylicacid, 1-(9H-fluoren-9-ylMethyl) ester, (2S)
(S)-1,2-Piperidinedicarboxylic acid 1-(9H-fluoren-9-ylmethyl) ester
N-(9-Fluorenyloxycbonyl)-piperidine-2R-cboxylicacid
FMOC-PIP-OH
FMOC-L-HOMOPROLINE
Fmoc-L-PIPE
FMOC-L-PIPECOLIC ACID //BP
FMOC-HOMOPRO-OH
N-FMoc-L-pipecolic acid
FMOC-L-PIPECOLIC ACID
Description Fmoc-HoPro-OH is a proline 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.

Density 1.293±0.06 g/cm3
Boiling Point 553.7±50.0 °C at 760 mmHg
Melting Point 161-162.5 ºC
Molecular Formula C21H21NO4
Molecular Weight 351.396
Flash Point 288.7±30.1 °C
Exact Mass 351.147064
PSA 66.84000
LogP 3.92
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.608
Storage condition 2-8°C
Water Solubility Insuluble (8.8E-3 g/L) (25 ºC)
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
RIDADR UN 3077 9 / PGIII
WGK Germany 3
HS Code 2933399090
HS Code 2933399090
Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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