7510-43-2 Usage
Appearance
White to off-white solid
The compound is a solid with a pale color, ranging from pure white to a slightly darker off-white shade.
Chemical classification
Hydrazinecarboxamide derivative
It belongs to the class of compounds known as hydrazinecarboxamides, which are characterized by the presence of a hydrazine group (NH2) and a carboxamide group (CONH2) in their structure.
Substituent
2,6-dimethylheptan-4-ylidene
The hydrazinecarboxamide core of the compound is substituted with a 2,6-dimethylheptan-4-ylidene group, which consists of a seven-carbon chain with two methyl groups (CH3) attached to the second and sixth carbon atoms, and a double bond between the fourth and fifth carbon atoms.
Potential applications
Pharmaceutical or chemical industries
Due to its unique structural features, 2-(2,6-dimethylheptan-4-ylidene)hydrazinecarboxamide may have potential uses in the pharmaceutical or chemical industries, such as in the development of new drugs or chemical processes.
Further research and testing required
To fully understand its properties and potential uses
More studies and experiments are needed to explore the compound's properties, reactivity, and potential applications, as its behavior and utility are not yet fully known.
Check Digit Verification of cas no
The CAS Registry Mumber 7510-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7510-43:
(6*7)+(5*5)+(4*1)+(3*0)+(2*4)+(1*3)=82
82 % 10 = 2
So 7510-43-2 is a valid CAS Registry Number.
7510-43-2Relevant articles and documents
MULTINUCLEAR MAGNETIC RESONANCE AND RELATED STUDIES ON AZOMETHINE BORON COMPLEXES OF SEMICARBAZONES AND THIOSEMICARBAZONES
Bhal, L.,Singh, R. V.,Tandon, J. P.
, p. 251 - 260 (2007/10/02)
Synthetic and stereochemical features of some interesting boron complexes have been described.These three and four coordinated complexes have been prepared by the interaction of 2-isopropoxy-1, 3,2-benzodioxaborole with semicarbazones and thiosemicarbazones having the donor sets NOH and NSH in unimolar ratio and with semicarbazones and thiosemicarbazones having the donor sets HONOH and OHNSH in 1:1 and 2:1 molar ratios.Depending on the stoichiometry of the reactions, different moles of isopropanol are liberated and a variety of new boron azomethine complexes are obtained.On the basis of IR, (1)H NMR, (11)B NMR and (13)C NMR data plausible geometries have been proposed for the resulting derivatives, X-ray powder diffraction studies of a representative compound have also been carried out and the results show that adopts 'orthorhombic' type of lattice with unit cell dimensions; a= 10.84 Angstroem, b= 24.12 Angstroem, and c= 28.74 Angstroem.
