CAS Number28782-78-7
SynonymsBoc-L-Ala-Gly-OH; N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]glycine; (S)-2-(2-((tert-Butoxycarbonyl)amino)propanamido)acetic acid; Glycine,N-[(1,1-diMethylethoxy)carbonyl]-L-alanyl; N-(tert-butyloxycarbonyl)-(S)-alanylglycine; 2-((2S)-2-((tert-butoxycarbonyl)amino)propanamido)acetic acid; (S)-2-(2-(tert-butoxycarbonylamino)propanamido)acetic acid; L-BocAlaGlyOH; N-tert-butyloxycarbonyl-L-alanyl-glycine
Molecular FormulaC10H18N2O5
Molecular Weight246.26
Purity96+%
Density1.19g/cm3
Boiling Point484.4ºC at 760mmHg
EINECS0
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 28782-78-7 |
| Catalog No. | 2A-0151446 |
| Chinese Name | 叔丁氧羰基-丙氨酰-甘氨酸 |
| Synonyms | Boc-L-Ala-Gly-OH; N-[N-[(1,1-dimethylethoxy)carbonyl]-L-alanyl]glycine; (S)-2-(2-((tert-Butoxycarbonyl)amino)propanamido)acetic acid; Glycine,N-[(1,1-diMethylethoxy)carbonyl]-L-alanyl; N-(tert-butyloxycarbonyl)-(S)-alanylglycine; 2-((2S)-2-((tert-butoxycarbonyl)amino)propanamido)acetic acid; (S)-2-(2-(tert-butoxycarbonylamino)propanamido)acetic acid; L-BocAlaGlyOH; N-tert-butyloxycarbonyl-L-alanyl-glycine |
| Molecular Formula | C10H18N2O5 |
| Molecular Weight | 246.26 |
| Purity | 96+ |
| Density | 1.19g/cm3 |
| Boiling Point | 484.4ºC at 760mmHg |
| Storage Condition | 2-8°C |
| Application | (S)-2-(2-((tert-butoxycarbonyl)amino)propionamide)acetic acid is a derivative of glycine (HY-Y0966) [1]. |
| EINECS | 0 |
| HTC | 2924199090 |
| UN(IATA) | 0 |
| PubChem ID | 29300817 |
| SMILES | CC(NC(=O)OC(C)(C)C)C(=O)NCC(=O)O |
| InChI | InChI=1S/C10H18N2O5/c1-6(8(15)11-5-7(13)14)12-9(16)17-10(2,3)4/h6H,5H2,1-4H3,(H,11,15)(H,12,16)(H,13,14) |
| InChI Key | PBGVVLQMNSPMKN-LURJTMIESA-N |
| Use of | (S)-2-(2-((tert-Butoxycarbonyl)amino)propanamido)acetic acid is a Glycine (HY-Y0966) derivative[1]. Properties Name boc-ala-gly-oh Synonym More Synonyms Boc-Ala-Gly-OH Biological Activity Description (S)-2-(2-((tert-Butoxycarbonyl)amino)propanamido)acetic acid is a Glycine (HY-Y0966) 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):1793-1144. Chemical & Physical Properties Molecular Formula C10H18N2O5 Exact Mass 246.12200 PSA 104.73000 LogP 0.88220 Index of Refraction 1.48 InChIKey PBGVVLQMNSPMKN-LURJTMIESA-N SMILES CC(NC(=O)OC(C)(C)C)C(=O)NCC(=O)O Safety Information Hazard Codes Xi HS Code 2924199090 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 30.0% |
| Transport Info | Product name: Summary 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
| Related Products in Biotechnology & Diagnostics | ||
|---|---|---|
| BOC-5-AMINO-3-OXAPENTANOIC ACID.DCHA | 142929-49-5 | 2A-0151438 |
| BOC-6-AMINOCAPROIC ACID | 6404-29-1 | 2A-0151440 |
| BOC-8-AMINO-3,6-DIOXAOCTANOIC ACID DCHA | 560088-79-1 | 2A-0151441 |
| BOC-8-AOC-OH | 30100-16-4 | 2A-0151442 |
| BOC-A-PROPYL-DL-PROLINE | 351002-88-5 | 2A-0151444 |
| BOC-ALA-N(OCH3)CH3 | 87694-49-3 | 2A-0151447 |
| BOC-AMCP-OH | 204376-48-7 | 2A-0151449 |
| BOC-ARG.HCL.H2O | 204070-00-8 | 2A-0151454 |
| BOC-ASP-NH2 | 74244-17-0 | 2A-0151462 |
| BOC-BETA-HOARG(TOS)-OH | 136271-81-3 | 2A-0151466 |
| Browse all Biotechnology & Diagnostics products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA
EN
SDS