925-83-7 Usage
General Description
Sebacic dihydrazide is a chemical compound primarily used in various manufacturing processes due to its properties as a curing agent. This white, crystalline substance has the molecular formula C10H20N4O2 and is often used in the production of epoxy resin systems, rubber, adhesives, and coatings, among others. Due to its functionality as a hardener and cross-linking agent, it helps improve the heat stability, mechanical properties, and water resistance of various products. More research is necessary to determine the potential environmental or health consequences relating to this compound's exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 925-83-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 925-83:
(5*9)+(4*2)+(3*5)+(2*8)+(1*3)=87
87 % 10 = 7
So 925-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H22N4O2/c11-13-9(15)7-5-3-1-2-4-6-8-10(16)14-12/h1-8,11-12H2,(H,13,15)(H,14,16)
925-83-7Relevant articles and documents
-
Korshak et al.
, (1967)
-
Synthesis of novel bis-1,3,4-thiadiazoles, bis-1,2,4-triazoles and their antimicrobial activity
Burghate, Megha K.,Burghate,Berad
body text, p. 561 - 565 (2009/08/15)
Condensation of scbacic acid dihydrazide (1) with aryl/alkyl isothiocyanates (2a-g) gives bis-(N-aryl/alkylthiocarbamido)-scbacic acid diamides (3a-g), which on reaction with o-phosphoric acid yields l,8-bis-(2-aryl/alkylamino-l,3,4-thiadiazol-5-yl)-octanes (4a-g). 1,8-Bis-(3-mercapto-4-aryl/alkyl-1,2,4-triazol-5-yl)-octanes (5a-g) were obtained by a similar condensation of compounds (3a-g) with aqueous KOH, which on reaction with ethyl iodide in the form of dihydroiodides have been isolated (6a-g). These on basification with aq. ammonia solution afforded free bases (7a-g). Compounds (4a-g) on benzoylation with benzoyl chloride and NaOH affords benzoyl derivatives (8a-g). The structures of all these compounds were confirmed on the basis of elemental analysis and spectral data and evaluated for their antimicrobial activity against gram positive and gram negative bacteria.
