N-(5-Amino-1H-tetrazol-1-yl)formamide

被引:2
|
作者
He, Chun-Lin [1 ]
Du, Zhi-Ming [1 ]
Tang, Zheng-Qiang [1 ]
Cong, Xiao-Min [1 ]
Meng, Ling-Qiao [1 ]
机构
[1] Beijing Inst Technol, State Key Lab Explos Sci & Technol, Beijing 100081, Peoples R China
关键词
DERIVATIVES;
D O I
10.1107/S1600536809044833
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
In the title compound, C2H4N6O, the planar [maximum deviation = 0.006 (2) angstrom] aminotetrazole group makes a dihedral angle of 83.65 (8)degrees with the formamide unit. In the crystal structure, intermolecular N-H center dot center dot center dot N, N-H center dot center dot center dot O and C-H center dot center dot center dot N hydrogen bonds are responsible for the formation of a three-dimensional network.
引用
收藏
页码:O2901 / U2202
页数:7
相关论文
共 50 条
  • [11] Efficient syntheses of polyamines bearing 1H-tetrazol-5-yl units on their amino functions
    Athanassopoulos, Constantinos M.
    Garnelis, Thomas
    Magoulas, George
    Papaioannou, Dionissios
    SYNTHESIS-STUTTGART, 2006, 18 (18): : 3134 - 3140
  • [12] 4-(1H-Tetrazol-5-yl)-1H-indole
    Ge, Yu-Hua
    Han, Pei
    Wei, Ping
    Ouyang, Ping-Kai
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2010, 66 : O2390 - U1001
  • [13] 2-(1H-tetrazol-5-yl)benzonitrile
    Xing, Zheng
    Han, Guang-Fan
    Zhu, Wei-Feng
    Zhao, Yu-Yuan
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2008, 64 : O816 - U1528
  • [14] Synthesis, Docking and Antibacterial Evaluation of N-(1-(3-Fluoro-4-morpholinophenyl)-1H-tetrazol-5-yl) Amides
    Boddapati, S. N. Murthy
    Kola, A. Emmanuel
    Talari, Subrahmanyam
    Arnipalli, Manikanta Swamy
    CHEMISTRY AFRICA-A JOURNAL OF THE TUNISIAN CHEMICAL SOCIETY, 2022, 5 (03): : 781 - 790
  • [15] Synthesis, Docking and Antibacterial Evaluation of N-(1-(3-Fluoro-4-morpholinophenyl)-1H-tetrazol-5-yl) Amides
    S. N. Murthy Boddapati
    A. Emmanuel Kola
    Subrahmanyam Talari
    Manikanta Swamy Arnipalli
    Chemistry Africa, 2022, 5 : 781 - 790
  • [16] Bis[(1-methyl-1H-tetrazol-5-yl)sulfanyl]ethane
    Li, Chun-Rong
    Chen, Tao
    Xia, Zheng-Qiang
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2011, 67 : O1669 - U523
  • [17] Bis[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methane
    Wei, Wei
    Xia, Zheng-qiang
    Chen, San-ping
    Gao, Sheng-li
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2011, 67 : O999 - U1602
  • [18] Synthesis of novel N-aryl-N-(1H-tetrazol-5-yl)benzenesulfonamides in water
    Nasrollahzadeh, Mahmoud
    Motahharifar, Narjes
    APPLIED ORGANOMETALLIC CHEMISTRY, 2020, 34 (08)
  • [19] 3-(1H-Tetrazol-5-yl)pyridinium 3-(2H-tetrazol-5-yl)pyridinium dinitrate
    Cui, Li-Jing
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2009, 65 : 01684 - U3360
  • [20] Selective synthesis of pyrazolo[3,4-d]pyrimidine, N-(1H-pyrazol-5-yl) formamide, or N-(1H-pyrazol-5-yl)formamidine derivatives from N-1-substituted-5-aminopyrazoles with new Vilsmeier-type reagents
    Chang, Chun-Hsi
    Tsai, Henry J.
    Huang, Yu-Ying
    Lin, Hui-Yi
    Wang, Li-Ya
    Wu, Tian-Shung
    Wong, Fung Fuh
    TETRAHEDRON, 2013, 69 (04) : 1378 - 1386