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13730-91-1

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13730-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13730-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,3 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13730-91:
(7*1)+(6*3)+(5*7)+(4*3)+(3*0)+(2*9)+(1*1)=91
91 % 10 = 1
So 13730-91-1 is a valid CAS Registry Number.
InChI:InChI=1/B2H10N2/c1-3-4-2/h3-4H2,1-2H3

13730-91-1Relevant academic research and scientific papers

Preparation and dehydrogenation properties of lithium hydrazidobis(borane) (LiNH(BH3)NH2BH3)

Fu, He,Yang, Junzhi,Wang, Xiaojuan,Xin, Gongbiao,Zheng, Jie,Li, Xingguo

, p. 7334 - 7339 (2014)

LiNH(BH3)NH2BH3, the first example of metal-substituted hydrazine bisborane (HBB), is synthesized via the reaction between HBB and n-butyllithium in ether solution. 11B NMR and Fourier transform infrared spectroscopy indicate a new structure, in which one of the N-H bonds is replaced by a N-Li bond. The X-ray diffraction pattern of the product also indicates the formation of a new crystal structure. This compound releases hydrogen at 126 and 170 °C with satisfactory purity and exhibits superior hydrogen storage properties compared with HBB. Differential scanning calorimetry measurement suggests the dehydrogenation reaction of this compound is less exothermic than that of HBB.

Spectroscopic Studies on Hydrazine-Boranes, Key Compounds for Chemical Hydrogen Storage

Escalona, Javier Torres,Guillemin, Jean-Claude,Darrigan, Clovis,Chrostowska, Anna

, p. 6003 - 6015 (2019)

Hydrazine-boranes (H2NNH2·BH3 and H3B·NH2NH2·BH3) have been proposed for the storage of hydrogen, but these compounds have not created scope for extensive research works as ammonia- A nd methylamine-boranes have made these last decades. In the exciting research devoted to energy storage with environmentally friendly processes, hydrazine-borane, hydrazine-bisborane, and their simply substituted derivatives could provide a satisfactory response for hydrogen production and recyclability of the formed products. To date, knowledge of the physical and chemical properties of these compounds is still scarce. In this paper, the electronic structure of various hydrazine-boranes complexes is studied by ultraviolet-photoelectron spectroscopy (UV-PES), which is the experimental technique giving direct access to the energy of occupied molecular orbitals. Thus, UV-PE spectra were registered and first ionization energies were determined. Understanding of different types of interactions between nitrogen lone pairs and their variations by complexation has been our essential goal in these studies. In particular, clear stabilization of all molecular orbital energies is noted when complexation with borane takes place. Evolution of the σBN bond during the hydrogen release process upon thermal activation has also been studied experimentally by UV-PES and supported by quantum chemical calculations.

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