45530-21-0 ((2,5-Oxazolidinedione,4-methyl-, (-)-)

快速询单

结构式：

2,5-Oxazolidinedione,4-methyl-, (-)-MOL文件

CAS号：

45530-21-0

英文名称：

2,5-Oxazolidinedione,4-methyl-, (-)-

分子式：

C₄H₅NO₃

分子量：

115.087401151657

2,5-Oxazolidinedione,4-methyl-, (-)-(45530-21-0)名称与标识符

名称

中文别名：

DL-丙氨酸-N-羧基-环内酸酐;

英文别名：

2,5-Oxazolidinedione,4-methyl-, (-)-;2,5-Oxazolidinedione,4-methyl-,(-)-(9CI);(+-)-4-Methyl-oxazolidin-2,5-dion;(+-)-4-methyl-oxazolidine-2,5-dione;4-methyl-oxazolidine-2,5-dione;AC1L2ASB;AG-E-91520;alanine-N-carboxy anhydride;Butanedioicacid, hydroxy-, zinc salt (1:1) (9CI);CTK1A6243;DL-4-methyl-1,3-oxazolidine-2,5-dione;DL-Aepfelsaeure,;DL-alanine-N-carboxanhydride;EINECS 220-647-4;MALIC ACID, ZINC SALT;Malic acid, zinc salt (1:1) (8CI);N-carboxyanhydrides of alanine;zinc malate;Zincmalate (7CI);30291-41-9;MFCD03411277;45530-21-0;CS-0328034;AKOS016014681;FT-0698464;2-Hydroxy-4-methyl-1,3-oxazol-5(4H)-one;NSC524103;EINECS 250-114-1;EINECS 214-759-2;NSC-524103;DL-Alanine-N-carboxy anhydride;L-Alanine N-carboxyanhydride;4-methyl-1,3-oxazolidine-2,5-dione;NS00079515;Ala-NCA;FT-0698196;SCHEMBL280456;FD21041;(1)-4-Methyloxazolidine-2,5-dione;2,5-oxazolidinedione, 4-methyl-;FT-0689536;SY103956;BCP18817;J-650094;4-Methyloxazolidine-2,5-dione;1192-73-0;DTXSID90922888;

标识符

InChIKey：

DTETYCNJKAUROO-UHFFFAOYSA-N

Inchi：

1S/C4H5NO3/c1-2-3(6)8-4(7)5-2/h2H,1H3,(H,5,7)

SMILES：

O1C(NC(C1=O)C)=O

2,5-Oxazolidinedione,4-methyl-, (-)-(45530-21-0)物化性质

实验特性

折射率 : 1.447
沸点 : °Cat760mmHg
闪点 : °C
密度 : 1.296

计算特性

精确分子量 : 115.027
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 0
同位素质量 : 115.027
重原子数量 : 8
复杂度 : 142
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） : -0.1
拓扑分子极性表面积 : 55.4A^2

2,5-Oxazolidinedione,4-methyl-, (-)-(45530-21-0)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
南通众合化工新材料有限公司	18762756250 0513-55074056	胡经理	2369399482		询单
南通众合化工新材料有限公司	18762756250 0513-55074056	胡经理	2369399482		询单

2,5-Oxazolidinedione,4-methyl-, (-)-(45530-21-0)相关文献

1. Synthetic enzymes. Part 2. Catalytic asymmetric epoxidation by means of polyamino-acids in a triphase system
Sebastián Juliá,Joan Guixer,Jaume Masana,José Rocas,Stefano Colonna,Rita Annuziata,Henriette Molinari J. Chem. Soc. Perkin Trans. 1 1982 1317
2. α-Aminoacyl derivatives of aminobenzoic acid and of amino-oxy-acids by reaction of their hydrochlorides with amino-acid N-carboxyanhydrides
Y. Knobler,S. Bittner,D. Virov,Max Frankel J. Chem. Soc. C 1969 1821
3. A poloxamer-polypeptide thermosensitive hydrogel as a cell scaffold and sustained release depot
Ji-Yu Lin,Po-Liang Lai,Yuan-Kai Lin,Sydney Peng,Li-Yu Lee,Chieh-Nan Chen,I-Ming Chu Polym. Chem. 2016 7 2976
4. 749. Reaction of N-carboxy-α-amino-acid anhydrides with hydrochlorides of hydroxylamine, O-alkylhydroxylamines, and amines; syntheses of amino-hydroxamic acids, amido-oxy-peptides, and α-amino-acid amides
Yehuda Knobler,Shmuel Bittner,Max Frankel J. Chem. Soc. 1964 3941
5. Multi-responsive polypeptide hydrogels derived from N-carboxyanhydride terpolymerizations for delivery of nonsteroidal anti-inflammatory drugs
Jingwei Fan,Richen Li,Hai Wang,Xun He,Tan P. Nguyen,Rachel A. Letteri,Jiong Zou,Karen L. Wooley Org. Biomol. Chem. 2017 15 5145
6. Copolymers containing carbohydrates and other biomolecules: design, synthesis and applications
Zhiyuan Ma,X. X. Zhu J. Mater. Chem. B 2019 7 1361
7. Peptide-directed assembly of functional supramolecular polymers for biomedical applications: electroactive molecular tongue-twisters (oligoalanine–oligoaniline–oligoalanine) for electrochemically enhanced drug delivery
John G. Hardy,Megan N. Amend,Sydney Geissler,Vincent M. Lynch,Christine E. Schmidt J. Mater. Chem. B 2015 3 5005
8. Polymer–protein conjugates: an enzymatic activity perspective
Marc A. Gauthier,Harm-Anton Klok Polym. Chem. 2010 1 1352
9. 1216. Studies on some O-acyl N-substituted hydroxylamines
P. G. Sammes J. Chem. Soc. 1965 6608

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960化工网为您提供2,5-Oxazolidinedione,4-methyl-, (-)-专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.45530-21-0,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:45530-21-0 国际站:45530-21-0