730-29-0 Usage
Chemical class
Aromatic amine
Functional groups
Contains a nitro group and two amine groups
Reactivity
Highly reactive due to the presence of the nitro group
Applications
a. Manufacturing of dyes and pigments
b. Laboratory research as a reagent in organic synthesis
c. Found in some pharmaceutical formulations
Toxicity
Toxic and can have harmful effects on human health
Health hazards
a. Skin and eye irritation
b. Classified as a potential carcinogen
Safety precautions
Proper safety protocols should be followed when handling this compound
Physical state
Likely a solid, though specific information on physical state is not provided in the material
Appearance
The material does not provide information on the appearance of the compound
Solubility
The material does not provide information on the solubility of the compound
Melting point
The material does not provide information on the melting point of the compound
Boiling point
The material does not provide information on the boiling point of the compound
Density
The material does not provide information on the density of the compound
Molecular weight
The material does not provide the molecular weight of the compound
Check Digit Verification of cas no
The CAS Registry Mumber 730-29-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 730-29:
(5*7)+(4*3)+(3*0)+(2*2)+(1*9)=60
60 % 10 = 0
So 730-29-0 is a valid CAS Registry Number.
730-29-0Relevant articles and documents
Three-Way Chemoselectivity Switching through Coupled Equilibria
Puangsamlee, Thamon,Miljani?, Ognjen ?.
supporting information, p. 5900 - 5904 (2020/08/05)
Controlling the chemoselectivity of reactions operating on complex mixtures, including those found in biological and petrochemical feedstocks or in the primordial soup from which life emerged, is generally challenging. The selectivity of imine oxidation c
Remarkable Acceleration of Benzimidazole Synthesis and Cyanosilylation Reactions in a Supramolecular Solid Catalyst
Rojas-Buzo, Sergio,García-García, Pilar,Corma, Avelino
, p. 997 - 1004 (2017/03/27)
A solid metal–organic catalyst with hydrophobic pockets and Lewis acid centers strongly accelerates the reaction rate for organic reactions. This is exemplified for the cyanosilylation of ketones and for the synthesis of benzimidazoles, for which very hig
An efficient and environmental benign synthesis of 2-benzimidazoles and 2-benzothiazoles using CeCl3-NaI as catalyst
Zhu, Xun,Wei, Yunyang
, p. 119 - 121 (2013/04/23)
A one-pot condensation of an aldehyde with 1,2-phenylenediamine or 2-aminothiophenol in dimethyl carbonate at 100°C under O2 in the presence of catalytic amounts of CeCl3-NaI gave an imine intermediate, which cyclised and dehydrogenated to give 2-arylbenzimidazoles or 2-arylbenzothiazoles in good yields.
