L-Alanylglycine methyl ester
Modify Date: 2024-01-09 14:12:54
L-Alanylglycine methyl ester structure
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Common Name | L-Alanylglycine methyl ester | ||
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| CAS Number | 51513-59-8 | Molecular Weight | 160.17100 | |
| Density | 1.135 | Boiling Point | 296ºC | |
| Molecular Formula | C6H12N2O3 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 133ºC | |
Use of L-Alanylglycine methyl esterMethyl L-alanylglycinate is a Glycine (HY-Y0966) derivative[1]. |
| Name | (S)-Methyl 2-(2-aminopropanamido)acetate |
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| Synonym | More Synonyms |
| Description | Methyl L-alanylglycinate is a Glycine (HY-Y0966) derivative[1]. |
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| 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 | 1.135 |
|---|---|
| Boiling Point | 296ºC |
| Molecular Formula | C6H12N2O3 |
| Molecular Weight | 160.17100 |
| Flash Point | 133ºC |
| Exact Mass | 160.08500 |
| PSA | 81.42000 |
| Index of Refraction | 1.461 |
| HS Code | 2924199090 |
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L-Alanylglycine... CAS#:51513-59-8 |
| Literature: Khalikov, Sh. Kh.; Alieva, S. V.; Ashurov, S. G. Russian Journal of Bioorganic Chemistry, 1994 , vol. 20, # 4 p. 202 - 212 Bioorganicheskaya Khimiya, 1994 , vol. 20, # 4 p. 393 - 405 |
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L-Alanylglycine... CAS#:51513-59-8 |
| Literature: Kokan, Zoran; Kirin, Srecko I. European Journal of Organic Chemistry, 2013 , # 36 p. 8154 - 8161 |
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L-Alanylglycine... CAS#:51513-59-8 |
| Literature: Johnson,B.J.; Trask,E.G. Journal of the Chemical Society [Section] C: Organic, 1969 , p. 2644 - 2647 |
| Precursor 2 | |
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| DownStream 0 | |
| HS Code | 2924199090 |
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| 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% |
| methyl 2-[[(2S)-2-aminopropanoyl]amino]acetate |