CAS Number177966-58-4
Synonyms(2S)-3-(3,4-Dichlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; FMOC-D-3,4-Dichl; FMOC-D-3,4-DICHLOROPHENYLALANINE; Fmoc-L-phe(3,4-Cl2)-OH; FMOC-3,4-DICHLORO-D-PHE-OH; MFCD00273472; RARECHEM BK PT 0120; 3,4-Dichloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine; Fmoc-D-Phe(3,4-Cl2)-OH; 3,4-Dichloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine; FMOC-D-PHE(3,4-DI-CL)-OH; FMOC-D-3,4-DICHLORO-PHE-OH; (2R)-3-(3,4-Dichlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; FMOC-D-3,4-DICHLOROPHE; FMOC-D-PHE(M,P-CL2)-OH; FMOC-(3,4-DI-CL)-D-PHE-OH; Fmoc-D-Phe(3,4-DiCl)-OH
Molecular FormulaC24H19Cl2NO4
Molecular Weight447.48
Density1.4±0.1 g/cm3
Boiling Point661.7±55.0 °C at 760 mmHg
Melting Point122ºC
Appearancesolid
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 177966-58-4 |
| Catalog No. | 2A-9085480 |
| Chinese Name | FMOC-D-3,4-二氯苯丙氨酸 |
| Synonyms | (2S)-3-(3,4-Dichlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; FMOC-D-3,4-Dichl; FMOC-D-3,4-DICHLOROPHENYLALANINE; Fmoc-L-phe(3,4-Cl2)-OH; FMOC-3,4-DICHLORO-D-PHE-OH; MFCD00273472; RARECHEM BK PT 0120; 3,4-Dichloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine; Fmoc-D-Phe(3,4-Cl2)-OH; 3,4-Dichloro-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-phenylalanine; FMOC-D-PHE(3,4-DI-CL)-OH; FMOC-D-3,4-DICHLORO-PHE-OH; (2R)-3-(3,4-Dichlorophenyl)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid; FMOC-D-3,4-DICHLOROPHE; FMOC-D-PHE(M,P-CL2)-OH; FMOC-(3,4-DI-CL)-D-PHE-OH; Fmoc-D-Phe(3,4-DiCl)-OH |
| Molecular Formula | C24H19Cl2NO4 |
| Molecular Weight | 447.48 |
| Density | 1.4±0.1 g/cm3 |
| Boiling Point | 661.7±55.0 °C at 760 mmHg |
| Melting Point | 122ºC |
| Appearance | solid |
| Storage Condition | 2-8°C, sealed, dry |
| Application | Fmoc-D-Phe(3,4-DiCl)-OH is a phenylalanine derivative [1]. |
| HTC | 2924299090 |
| PubChem ID | 329791236 |
| MDL Number | MFCD01317731 |
| SMILES | COc1ccc(C[C@@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)cc1OC |
| InChI | 1S/C26H25NO6/c1-31-23-12-11-16(14-24(23)32-2)13-22(25(28)29)27-26(30)33-15-21-19-9-5-3-7-17(19)18-8-4-6-10-20(18)21/h3-12,14,21-22H,13,15H2,1-2H3,(H,27,30)(H,28,29)/t22-/m1/s1 |
| InChI Key | XJRGWWYKCGWQHH-JOCHJYFZSA-N |
| NACRES Code | NA.21 |
| UNSPSC | 12352209 |
| MSDS | msds/85480_1_177966_58_4.pdf |
| Bioactivity | Fmoc-D-Phe(3,4-DiCl)-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):1793-945. Chemical & Physical Properties Density 1.4±0.1 g/cm3 Boiling Point 661.7±55.0 °C at 760 mmHg Melting Point 122ºC Molecular Formula C24H19Cl2NO4 Molecular Weight 456.318 Flash Point 354.0±31.5 °C Exact Mass 455.069122 PSA 75.63000 LogP 6.47 Vapour Pressure 0.0±2.1 mmHg at 25°C Index of Refraction 1.642 InChIKey QNVHCYWPXIGFGN-JOCHJYFZSA-N SMILES O=C(NC(Cc1ccc(Cl)c(Cl)c1)C(=O)O)OCC1c2ccccc2-c2ccccc21 |
| Use of | Fmoc-D-Phe(3,4-DiCl)-OH is a phenylalanine derivative[1]. Properties Name Fmoc-3,4-dichloro-D-phenylalanine Synonym More Synonyms Fmoc-L-phe(3,4-Cl2)-OH Biological Activity Description Fmoc-D-Phe(3,4-DiCl)-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):1793-945. Chemical & Physical Properties Exact Mass 455.069122 PSA 75.63000 Index of Refraction 1.642 InChIKey QNVHCYWPXIGFGN-JOCHJYFZSA-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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