3391-07-9 Usage
Description
7-NORBORNYL TERT-BUTYL ETHER, also known as 7-tert-butyloxynorbornane, is a colorless liquid chemical compound with a strong odor. It is insoluble in water but soluble in organic solvents, and is known for its highly flammable nature and potential as a skin and eye irritant.
Uses
Used in Organic Synthesis:
7-NORBORNYL TERT-BUTYL ETHER is used as a solvent and a reagent in organic synthesis, facilitating various chemical reactions due to its unique properties.
Used in Biofuel Additives:
7-NORBORNYL TERT-BUTYL ETHER has been studied for its potential as a biofuel additive, which could enhance the performance and efficiency of biofuels.
Used as a Fuel Stabilizer:
It is also considered as a fuel stabilizer, helping to maintain the quality and stability of fuels over time.
Used in Polymer Production:
7-NORBORNYL TERT-BUTYL ETHER serves as a cross-linking agent in the production of polymers, contributing to the formation of three-dimensional networks that improve the material's properties.
Used in the Chemical Industry:
In the chemical industry, 7-NORBORNYL TERT-BUTYL ETHER is used as a versatile compound for various applications, including the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, due to its reactivity and solubility in organic solvents.
Check Digit Verification of cas no
The CAS Registry Mumber 3391-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3391-07:
(6*3)+(5*3)+(4*9)+(3*1)+(2*0)+(1*7)=79
79 % 10 = 9
So 3391-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-11(2,3)12-10-8-4-5-9(10)7-6-8/h8-10H,4-7H2,1-3H3
3391-07-9Relevant articles and documents
Franzus,Snyder
, p. 3423,3429 (1965)
Stereoselectivity in the rhodium-catalysed reductions of nonconjugated dienes
Nguyen, Bao,Brown, John M.
scheme or table, p. 1333 - 1343 (2009/12/27)
The stereochemical course of rhodium-catalysed addition of hydrogen and catecholborane to bicyclo[2.2.1]heptadiene, and of hydrogen to a range of cyclic dienes has been analysed. For hydroboration, the overall catalytic reaction possesses exo-selectivity, but the initial step is endo-selective. For hydrogenation (deuteration), the first step may occur with either exo- or endo- selectivity, depending on the structure of the diene. This enables a distinction to be made between pathways involving prior dissociation of the diene, and direct addition to the complexed diene without full dissociation. The relative ease of hydrogenation of the first and second doublebonds varies markedly with reactant structure, and also depends on the choice of catalyst ligands. For dicyclopentadiene, hydrogenation of the cyclopentene double bond is accompanied by rapid alkene isomerisation, as revealed by deuterium addition. The asymmetric hydrogenation of acyclic skipped mesodienes is reported, demonstrating control of relative rates of the two sequential steps, with ees of up to 53% after the first reduction.
