CAS Number198560-41-7
SynonymsFmoc-L-phe(2-Cl)-OH; MFCD00797578; Fmoc-D-phe(2-Cl)-OH; (2S)-3-(2-Chlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; Fmoc-2-chloro-L-phenylalanine; 2-Chloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine; Fmoc-L-2-Chlorophenylalanine; Fmoc-Phe(2-Cl)-OH; FMOC-L-2-Chlorophe
Molecular FormulaC24H20ClNO4
Molecular Weight421.87
Purity96+%
Density1.3±0.1 g/cm3
Boiling Point640.9±55.0 °C at 760 mmHg
Melting Point158ºC
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 198560-41-7 |
| Catalog No. | 2A-1155848 |
| Chinese Name | N-(9-芴甲氧羰酰基)-L-2-氯苯丙氨酸 |
| Synonyms | Fmoc-L-phe(2-Cl)-OH; MFCD00797578; Fmoc-D-phe(2-Cl)-OH; (2S)-3-(2-Chlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; Fmoc-2-chloro-L-phenylalanine; 2-Chloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine; Fmoc-L-2-Chlorophenylalanine; Fmoc-Phe(2-Cl)-OH; FMOC-L-2-Chlorophe |
| Molecular Formula | C24H20ClNO4 |
| Molecular Weight | 421.87 |
| Purity | 96+ |
| Density | 1.3±0.1 g/cm3 |
| Boiling Point | 640.9±55.0 °C at 760 mmHg |
| Melting Point | 158ºC |
| Storage Condition | 2-8C |
| Application | Fmoc Phe(2-Cl)-OH is a phenylalanine derivative [1]. |
| EINECS | 0 |
| HTC | 2924299090 |
| UN(IATA) | 0 |
| PubChem ID | 3189543 |
| MDL Number | MFCD00080281 |
| SMILES | O=C(NC(Cc1ccccc1Cl)C(=O)O)OCC1c2ccccc2-c2ccccc21 |
| InChI | InChI=1S/C24H20ClNO4/c25-21-12-6-1-7-15(21)13-22(23(27)28)26-24(29)30-14-20-18-10-4-2-8-16(18)17-9-3-5-11-19(17)20/h1-12,20,22H,13-14H2,(H,26,29)(H,27,28)/t22-/m0/s1 |
| InChI Key | RNNKPNPLIMFSDY-QFIPXVFZSA-N |
| NACRES Code | NA.22 |
| UNSPSC | 12352209 |
| Bioactivity | Fmoc-Phe(2-Cl)-OH is a phenylalanine derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others 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):1793-885. Chemical & Physical Properties Density 1.3±0.1 g/cm3 Boiling Point 640.9±55.0 °C at 760 mmHg Melting Point 158ºC Molecular Formula C24H20ClNO4 Molecular Weight 421.873 Flash Point 341.4±31.5 °C Exact Mass 421.108093 PSA 75.63000 LogP 6.00 Vapour Pressure 0.0±2.0 mmHg at 25°C Index of Refraction 1.638 InChIKey RNNKPNPLIMFSDY-QFIPXVFZSA-N SMILES O=C(NC(Cc1ccccc1Cl)C(=O)O)OCC1c2ccccc2-c2ccccc21 Storage condition 2-8C |
| Use of | Fmoc-Phe(2-Cl)-OH is a phenylalanine derivative[1]. Properties Name (2S)-3-(2-chlorophenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid Synonym More Synonyms FMOC-L-2-Chlorophe Biological Activity Description Fmoc-Phe(2-Cl)-OH is a phenylalanine derivative[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others 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):1793-885. Chemical & Physical Properties Exact Mass 421.108093 PSA 75.63000 Index of Refraction 1.638 InChIKey RNNKPNPLIMFSDY-QFIPXVFZSA-N |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: 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% |
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