6570-87-2 Usage
Uses
Used in Chemical Production:
3,4-Dimethyl-1-pentanol is used as a solvent and in the production of other chemicals, leveraging its chemical properties to facilitate reactions and processes in the synthesis of various compounds.
Used in Flavoring Agents for the Food Industry:
Capitalizing on its pleasant floral and fruity scent, 3,4-dimethyl-1-pentanol is utilized as a flavoring agent in the food industry, enhancing the taste and aroma of various food products.
Safety and Environmental Considerations:
Given its flammable nature and potential harmful effects if ingested or inhaled, 3,4-dimethyl-1-pentanol requires proper safety precautions during handling. Additionally, awareness of its environmental and health impacts is crucial to ensure responsible handling and disposal, minimizing any adverse effects on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 6570-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6570-87:
(6*6)+(5*5)+(4*7)+(3*0)+(2*8)+(1*7)=112
112 % 10 = 2
So 6570-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O/c1-6(2)7(3)4-5-8/h6-8H,4-5H2,1-3H3
6570-87-2Relevant academic research and scientific papers
Dual Rh?Ru Catalysts for Reductive Hydroformylation of Olefins to Alcohols
Rodrigues, Fábio M. S.,Kucmierczyk, Peter K.,Pineiro, Marta,Jackstell, Ralf,Franke, Robert,Pereira, Mariette M.,Beller, Matthias
, p. 2310 - 2314 (2018/07/31)
An active and selective dual catalytic system to promote domino hydroformylation–reduction reactions is described. Apart from terminal, di- and trisubstituted olefins, for the first time the less active internal C?C double bond of tetrasubstituted alkenes can also be utilized. As an example, 2,3-dimethylbut-2-ene is converted into the corresponding n-alcohol with high yield (90 %) as well as regio- and chemoselectivity (>97 %). Key for this development is the use of a combination of Rh complexes with bulky monophosphite ligands and the Ru-based Shvo's complex. A variety of aromatic and aliphatic alkenes can be directly used to obtain mainly linear alcohols.
