| Name | (2S)-4-oxo-4-phenylmethoxy-2-(phenylmethoxycarbonylamino)butanoic acid |
|---|---|
| Synonyms |
N-ALPHA-CBOBENZOXY-L-ASPTIC ACID BETA-BENZYL ESTER
4-Benzyl N-Carbobenzoxy-L-aspartate CBZ-L-ASPTIC ACID B-BENZYL ESTER N-ALPHA-CBZ-L-ASPTIC ACID BETA-BENZYL ESTER N-Benzyloxycarbonyl-L-Aspartic Acid 4-Benzyl Ester Z-L-aspartic acid 4-benzyl ester Z-L-Asp(Bzl)-OH N-CBZ-L-ASPTIC ACID 4-BENZYL ESTER Z-L-ASPTIC ACID B-BENZYLESTER MFCD00037820 N-Carbobenzoxy-L-aspartic Acid 4-Benzyl Ester N-Cbobenzoxy-L-asptic Acid 4-Benzyl Ester 4-Benzyl N-Cbz-L-asptate N-Cbz-L-asptic Acid 4-Benzyl Ester Z-Asp(OBzl)-OH Z-L-Asptic Acid-4-Benzyl Ester extrapure L-Aspartic acid, N-[(phenylmethoxy)carbonyl]-, 4-(phenylmethyl) ester Cbz-L-asptic acid - benzyl ester Z-Asp(OBzl)-OH, 10 mM in DMSO 4-Benzyl N-Cbz-L-aspartate CBZ-L-ASPTIC ACID BETA-BENZYL ESTER N-BENZYLOXYCBONYL-L-ASPTIC AC N-Cbz-L-Asptic acid 4-benzyl ester //BP N-CBOBENZOXY-L-ASPTIC-BETA-BENZYL ESTER (2S)-4-oxo-4-phenylmethoxy-2-(phenylmethoxycbonylamino)butanoicaci (2S)-4-(Benzyloxy)-2-{[(benzyloxy)carbonyl]amino}-4-oxobutanoic acid 4-(Phenylmethyl) hydrogen N-[(phenylmethoxy)carbonyl]-L-asptate N-[(PHENYLMETHOXY)carbonyl]-L-ASPTIC ACID 4-(PHENYLMETHYL) ESTER Z-L-Asptic acid-4-benzyl ester CBZ-ASP(OBZL)-OH Cbz-L-aspartic acid b-benzyl ester CBZ-OBzl)-OH N-Cbz-L-aspartic Acid 4-Benzyl Ester Z-ASPTIC ACID(OBZL)-OH N-Cbobenzoxy-L-asptic Acid 4-Benzyl Ester L-Asptic acid, N-[(phenylmethoxy)carbonyl]-, 4-(phenylmethyl) ester N-BENZYLOXYCBONYL-L-ASPTIC ACID 4-BENZYL ESTER Cbz-L-Asp (β-Bzl)OH N-Cbz-L-asptic acid β-benzyl ester Cbz-L-Asp(OBzl)-OH 4-benzyl hydrogen N-[(phenylmethoxy)carbonyl]-L-asptate 4-Benzyl N-Cbobenzoxy-L-asptate > N-Cbz-L-Aspartic acid 4-benzylester (2S)-4-oxo-4-phenylmethoxy-2-(phenylmethoxycbonylam N-Cbz-L-asptic acid β-benzyl ester, Z-L-asptic acid 4-benzyl ester Z-L-asptic acid -benzyl ester (assay) 4-Benzyl N-Cbobenzoxy-L-asptate N-Cbz-L-Asptic aci 4-oxo-4-phenylmethoxy-2-(phenylmethoxycbonylamino)butanoic acid (S)-2-(Benzyloxycbonylamino)succinic acid 4-benzyl ester Z-L-ASPTIC ACID BETA-BENZYL ESTER Z-ASP(OBZL)-OH (2S)-4-(benzyloxy)-2-{[(benzyloxy)carbonyl]amino}-4-oxobutanoic acid Asptic acid, N-[(phenylmethyl) -carbonyl]4-(phenylmethyl) ester N-cbobenzyloxy-L-asptic acid beta-benzyl ester N-BENZYLOXYCBONYL-L-ASPTIC ACID BETA-BENZYL ESTER (S)-4-(Benzyloxy)-2-(((benzyloxy)carbonyl)amino)-4-oxobutanoic acid N-alpha-Benzyloxycbonyl-L-asptic acid beta-benzyl ester 4-Benzyl N-Benzyloxycbonyl-L-asptate N-CBZ-L-ASPTIC ACID BETA-BENZYL ESTER EINECS 222-456-1 Z-Asptic acid,4-benzyl ester á-benzyl n-cbz-l-asptate (2S)-4-oxo-4-phenylmethoxy-2-(phenylmethoxycbonylamino)butanoic acid BENZYLOXYCBONYL-L-ASPTIC ACID BETA-BENZYL ESTER Z-L-asptic acid β-benzyl ester Z-Asptic Acid-O Benzyl Ester N-Cbz-L-Asparticacid4-benzylester Z-L-Asp(OBzl)-OH N-Cbobenzyloxy-L-asptic acid β-benzyl ester Z-L-ASPTIC ACID 4-BENZYL ESTER 4-Benzyl N-Cbz-L-asptate á-benzyl n-benzyloxycbonyl-l-asptate |
| Description | Z-Asp(OBzl)-OH is an aspartic acid 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 |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 587.4±50.0 °C at 760 mmHg |
| Melting Point | 105-107ºC |
| Molecular Formula | C19H19NO6 |
| Molecular Weight | 357.357 |
| Flash Point | 309.1±30.1 °C |
| Exact Mass | 357.121246 |
| PSA | 101.93000 |
| LogP | 3.86 |
| Vapour Pressure | 0.0±1.7 mmHg at 25°C |
| Index of Refraction | 1.581 |
| Storage condition | Store at RT. |
| Hazard Codes | Xi |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2924299090 |
|
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| Literature: Yamamoto, Yoshinori; Furuta, Toshiaki; Matsuo, Jiro; Kurata, Tetsuro Journal of Organic Chemistry, 1991 , vol. 56, # 20 p. 5737 - 5738 |
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| Literature: Yoshida, Masanori; Narita, Mao; Hara, Shoji Journal of Organic Chemistry, 2011 , vol. 76, # 20 p. 8513 - 8517 |
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| Literature: Jouin, P.; Castro, B.; Zeggaf, C.; Pantaloni, A.; Senet, J.P; et al Tetrahedron Letters, 1987 , vol. 28, # 15 p. 1665 - 1668 |
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| Literature: Jouin, P.; Castro, B.; Zeggaf, C.; Pantaloni, A.; Senet, J.P; et al Tetrahedron Letters, 1987 , vol. 28, # 15 p. 1665 - 1668 |
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| Literature: Journal of the American Chemical Society, , vol. 73, p. 4084,4087 |
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| Literature: Journal of the American Chemical Society, , vol. 73, p. 4084,4087 |
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| Literature: Journal of the Chemical Society, Perkin Transactions 1, , # 20 p. 3451 - 3459 |
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| Literature: Indian Journal of Chemistry, , vol. 3, p. 554 - 558 |
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| Literature: Tetrahedron Letters, , vol. 40, # 22 p. 4275 - 4278 |
| Precursor 9 | |
|---|---|
| DownStream 9 | |
| HS Code | 2924299090 |
|---|---|
| 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% |