141-73-1 Usage
Description
4-Methoxy-4-methyl-2-pentanol, also known as MMMP, is a colorless liquid chemical compound with the molecular formula C7H16O2. It has a pleasant odor and is commonly used as a solvent in various industries.
Uses
Used in Perfume Production:
4-Methoxy-4-methyl-2-pentanol is used as a solvent for the production of perfumes, providing a pleasant odor and enhancing the overall scent of the product.
Used in Pharmaceutical Manufacturing:
MMMP is utilized as a solvent in the production of pharmaceuticals, aiding in the manufacturing process and ensuring the quality of the final product.
Used in Flavoring and Fragrance Industry:
4-Methoxy-4-methyl-2-pentanol serves as a raw material in the creation of flavorings and fragrances, contributing to the unique scents and tastes of various consumer products.
Safety:
Although considered relatively non-toxic, it is important to handle 4-methoxy-4-methyl-2-pentanol with care and take proper protective measures when working with this compound to ensure safety for both human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 141-73-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141-73:
(5*1)+(4*4)+(3*1)+(2*7)+(1*3)=41
41 % 10 = 1
So 141-73-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c1-6(8)5-7(2,3)9-4/h6,8H,5H2,1-4H3/t6-/m1/s1
141-73-1Relevant articles and documents
Synthesis of bimetallic complexes bridged by 2,6-bis(benzimidazol-2-yl) pyridine derivatives and their catalytic properties in transfer hydrogenation
Günnaz, Salih,G?k?e, Ayta? Gürhan,Türkmen, Hayati
, p. 17317 - 17328 (2019/01/03)
A series of binuclear rhodium(i) and iridium(i) complexes with 2,6-bis(benzimidazol-2-yl) pyridine (bzimpy) derivatives were synthesized and characterized by elemental analysis and spectroscopic methods. The molecular and crystal structures of complex 3d were determined by the single crystal X-ray diffraction technique. Their monometallic analogues were prepared to compare the catalytic properties of the bimetallic complexes. To determine the catalyst properties that result in a cooperative, bimetallic enhancement of the reaction rate, the systematic variation of the intermetallic distance and the ligand donor properties of the bimetallic complexes were explored based on the transfer hydrogenation reactions of ketones.