39978-59-1 (丝氨酸乙酯,Serine, ethyl ester)

快速询单

结构式：

丝氨酸乙酯MOL文件

CAS号：

39978-59-1

中文名称：

丝氨酸乙酯

英文名称：

Serine, ethyl ester

分子式：

C₅H₁₁NO₃

分子量：

133.145741701126

丝氨酸乙酯(39978-59-1)名称与标识符

名称

中文别名：

丝氨酸乙酯;

英文别名：

Serine, ethyl ester;DL-serine ethyl ester;(?à)-Serineethyl ester;39978-59-1;GKCXXDSWWDWUHS-UHFFFAOYSA-N;Ethyl 2-amino-3-hydroxypropanoate;(S)-ETHYL 2-AMINO-3-HYDROXYPROPANOATE;SB47113;AKOS000265971;NCGC00337702-01;EN300-57608;AB00171994-03;AB46080;AKOS021982383;BS-9879;SCHEMBL818996;STL194158;ethyl (2S)-2-amino-3-hydroxy-propanoate;ethyl 2-amino-3-hydroxy-propanoate;

标识符

InChIKey：

GKCXXDSWWDWUHS-UHFFFAOYSA-N

Inchi：

1S/C5H11NO3/c1-2-9-5(8)4(6)3-7/h4,7H,2-3,6H2,1H3

SMILES：

O(CC)C(C(CO)N)=O

丝氨酸乙酯(39978-59-1)物化性质

计算特性

精确分子量 : 133.07389321g/mol
氢键供体数量 : 2
氢键受体数量 : 4
可旋转化学键数量 : 4
同位素质量 : 133.07389321g/mol
重原子数量 : 9
复杂度 : 94.2
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 1
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : -1.1
拓扑分子极性表面积 : 72.6Å²

丝氨酸乙酯(39978-59-1)推荐厂家更多厂家(2)

公司名称	手机号/电话	联系人	QQ	微信	询单
深圳振强生物技术有限公司	13670046396 86-755-66853366	颜经理	2851296953		询单
上海麦克林生化科技股份有限公司	15221275939 021-50706066	沈经理	269348414		询单

丝氨酸乙酯(39978-59-1)相关文献

1. 522. The β-phenylserine series. Part II
Ernst D. Bergmann,H. Bendas,Ch. Resnick J. Chem. Soc. 1953 2564
2. Towards a total synthesis of ulapualide A. Concise synthetic routes to the tris-oxazole ring system and tris-oxazole macrolide core in ulapualides, kabiramides, halichondramides, mycalolides and halishigamides
Shital K. Chattopadhyay,James Kempson,Alan McNeil,Gerald Pattenden,Michael Reader,David E. Rippon,David Waite J. Chem. Soc. Perkin Trans. 1 2000 2415
3. 260. Synthesis of some phosphorylated amino-hydroxy-acids and derived peptides related to the phosphoproteins
G. Riley,J. H. Turnbull,W. Wilson J. Chem. Soc. 1957 1373
4. Index of subjects
J. Chem. Soc. Abstr. 1924 126 ii1051
5. Synthesis and chemical reactivity of thiophenoxyphenylalanine bioisosteres, suitable synthons for the design of HIV protease inhibitors
G. Priem,L. Rocheblave,C. De Michelis,J. Courcambeck,J. L. Kraus J. Chem. Soc. Perkin Trans. 1 2000 819
6. 753. Interaction between carbonyl groups and biologically essential substituents. Part V. The effect of ketones on further series of optically active amino-derivatives
F. Bergel,Margaret A. Peutherer J. Chem. Soc. 1964 3965
7. Cationic pTyr/pSer imprinted polymers based on a bis-imidazolium host monomer: phosphopeptide recognition in aqueous buffers demonstrated by μ-liquid chromatography and monolithic columns
Celina Wierzbicka,Mingquan Liu,David Bauer,Knut Irgum,B?rje Sellergren J. Mater. Chem. B 2017 5 953
8. Index of subjects, 1947
J. Chem. Soc. 1947 1720
9. One-shot preparation of an inherently chiral trifunctional calix[4]arene from an easily available cone-triformylcalix[4]arene
Maria Ciaccia,Irene Tosi,Roberta Cacciapaglia,Alessandro Casnati,Laura Baldini,Stefano Di Stefano Org. Biomol. Chem. 2013 11 3642
10. Biomimetic peptide bond formation in water with aminoacyl phosphate esters
Raj S. Dhiman,Liliana Guevara Opinska,Ronald Kluger Org. Biomol. Chem. 2011 9 5645