CAS Number13171-93-2
SynonymsZ-Gly-Gly-L-Phe-OH; Cbz-Gly-Gly-L-Phe; N-benzyloxycarbonyl-glycylglycyl-L-phenylalanine; carbobenzoxyglycylglycyl-L-phenylalanine; Cbz-Gly-Gly-Phe-OH; N-benzyloxycarbonyl-L-glycyl-L-glycyl-L-phenylalanine; N-Cbz-glycylglycylphenylalanine
Molecular FormulaC21H23O6N3
Molecular Weight413.43
Purity96+%
Density1.301 g/cm3
Boiling Point771.2ºC at 760 mmHg
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 13171-93-2 |
| Catalog No. | 2A-1100882 |
| Chinese Name | Z-GLY-GLY-PHE-OH |
| Synonyms | Z-Gly-Gly-L-Phe-OH; Cbz-Gly-Gly-L-Phe; N-benzyloxycarbonyl-glycylglycyl-L-phenylalanine; carbobenzoxyglycylglycyl-L-phenylalanine; Cbz-Gly-Gly-Phe-OH; N-benzyloxycarbonyl-L-glycyl-L-glycyl-L-phenylalanine; N-Cbz-glycylglycylphenylalanine |
| Molecular Formula | C21H23O6N3 |
| Molecular Weight | 413.43 |
| Purity | 96+ |
| Density | 1.301 g/cm3 |
| Boiling Point | 771.2ºC at 760 mmHg |
| Storage Condition | Room temperature, sealed, dry |
| Application | Z-Gly-Gly-Phe-OH is an active compound. Z-Gly-Gly-Phe-OH can be used to synthesize enzymatic peptides [1]. |
| EINECS | 0 |
| HTC | 2934999090 |
| UN(IATA) | 0 |
| MDL Number | MFCD00055796 |
| SMILES | O=C(CNC(=O)OCc1ccccc1)NCC(=O)NC(Cc1ccccc1)C(=O)O |
| InChI | InChI=1S/C21H23N3O6/c25-18(12-23-21(29)30-14-16-9-5-2-6-10-16)22-13-19(26)24-17(20(27)28)11-15-7-3-1-4-8-15/h1-10,17H,11-14H2,(H,22,25)(H,23,29)(H,24,26)(H,27,28) |
| InChI Key | PARPWSYTROKYNG-UHFFFAOYSA-N |
| MSDS | msds/100882_1_13171_93_2.pdf |
| Use of | Z-Gly-Gly-Phe-OH is an active compound. Z-Gly-Gly-Phe-OH can be used for the synthesis of enzymic peptide[1]. Properties Name 3-phenyl-2-[[2-[[2-(phenylmethoxycarbonylamino)acetyl]amino]acetyl]amino]propanoic acid Synonym More Synonyms Z-Gly-Gly-Phe-OH Biological Activity Description Z-Gly-Gly-Phe-OH is an active compound. Z-Gly-Gly-Phe-OH can be used for the synthesis of enzymic peptide[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others References [1]. Kitaguchi. Hiroshi, et al. Enzymic peptide synthesis via segment condensation in the presence of water mimics. Journal of the American Chemical Society (1989), 111(26), 9272-3. Chemical & Physical Properties Molecular Formula C21H23N3O6 Exact Mass 413.15900 PSA 133.83000 LogP 2.01380 Index of Refraction 1.587 InChIKey PARPWSYTROKYNG-UHFFFAOYSA-N Safety Information HS Code 2934999090 Precursor & DownStream Precursor 5 CAS#:10466-61-2 H-Leu-NH2.HCl CAS#:169676-30-6 Z-Gly-Gly-L-Phe... CAS#:2899-60-7 CAS#:2566-19-0 N-[(Benzyloxy)c... DownStream 5 CAS#:100929-57-5 DES-TYR1-LEUCIN... CAS#:2566-19-0 N-[(Benzyloxy)c... CAS#:150-30-1 DL-Phenylalanine CAS#:6234-26-0 H-Gly-Gly-Phe-OH |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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