19775-89-4 ((4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-)

快速询单

结构式：

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-MOL文件

CAS号：

19775-89-4

英文名称：

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-

分子式：

C₂₂H₁₂

分子量：

276.33068

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-(19775-89-4)名称与标识符

名称

英文别名：

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-;

标识符

InChIKey：

XAKRHFYJDSMEMI-UHFFFAOYSA-N

Inchi：

InChI=1S/C22H12/c1-2-6-14-13(5-1)17-9-10-19-15-7-3-4-8-16(15)20-12-11-18(14)21(17)22(19)20/h1-12H

SMILES：

C1C=CC2C(=C3C=CC4=C5C=CC=CC5=C5C=CC=2C3=C45)C=1

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-(19775-89-4)物化性质

实验特性

折射率 : 1.648
沸点 : 472.2°Cat760mmHg
闪点 : 239.4°C
密度 : 1.443

计算特性

精确分子量 : 182.08
氢键供体数量 : 3
氢键受体数量 : 6
可旋转化学键数量 : 3
同位素质量 : 182.08
重原子数量 : 13
复杂度 : 187
同位素原子数量 : 0
确定原子立构中心数量 : 1
不确定原子立构中心数量 : 0
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

4-Pyrimidinepropanoicacid, a,2-diamino-, (aS)-(19775-89-4)相关文献

1. The synthesis of pyrimidin-4-yl substituted α-amino acids. A versatile approach from alkynyl ketones
Robert M. Adlington,Jack E. Baldwin,David Catterick,Gareth J. Pritchard J. Chem. Soc. Perkin Trans. 1 1999 855
2. A versatile approach to pyrimidin-4-yl substituted α-amino acids from alkynyl ketones; the total synthesis of l-lathyrine
Robert M. Adlington,Jack E. Baldwin,David Catterick,Gareth J. Pritchard acids from alkynyl ketones; the total synthesis of l-lathyrine. Robert M. Adlington Jack E. Baldwin David Catterick Gareth J. Pritchard Chem. Commun. 1997 1757
3. A versatile approach to pyrimidin-4-yl substituted α-amino acids from alkynyl ketones; the total synthesis of l-lathyrine
Robert M. Adlington,Jack E. Baldwin,David Catterick,Gareth J. Pritchard acids from alkynyl ketones; the total synthesis of l-lathyrine. Robert M. Adlington Jack E. Baldwin David Catterick Gareth J. Pritchard Chem. Commun. 1997 1757
4. A convenient synthesis of pyrimidinone and pyrimidine containing bisheteroarenes and analogs
Hardesh K. Maurya,Atul Gupta RSC Adv. 2014 4 22106
5. Chapter 5. Heterocylic chemistry
Andrew Marsh Annu. Rep. Prog. Chem. Sect. B: Org. Chem. 1998 94 155
6. The synthesis of novel heterocyclic substituted α-amino acids; further exploitation of α-amino acid alkynyl ketones
Robert M. Adlington,Jack E. Baldwin,David Catterick,Gareth J. Pritchard,Lam T. Tang J. Chem. Soc. Perkin Trans. 1 2000 303
7. Index pages
Nat. Prod. Rep. 1997 14 I1
8. The efficient, enantioselective synthesis of quinoxaline, pyrazine and 1,2,4-triazine substituted α-amino acids from vicinal tricarbonyls
Robert M. Adlington,Jack E. Baldwin,David Catterick,Gareth J. Pritchard J. Chem. Soc. Perkin Trans. 1 2001 668
9. Hot off the press
Robert A. Hill,Andrew R. Pitt Nat. Prod. Rep. 1997 14 1-iii
10. Chemical systematics
P. G. Waterman,A. I. Gray Nat. Prod. Rep. 1987 4 175

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