14548-60-8 Usage
Uses
Used in Pharmaceutical Industry:
(Benzyloxy)methanol is used as a chemical intermediate for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Dye Industry:
(Benzyloxy)methanol is used as a chemical intermediate in the production of dyes, enabling the creation of a wide range of colorants for various applications.
Used in Perfume Industry:
(Benzyloxy)methanol is used as a fragrance ingredient in perfumes, enhancing the scent profiles and providing a pleasant aroma.
Used in Cosmetic and Personal Care Products:
(Benzyloxy)methanol is used as a fragrance ingredient in cosmetic and personal care products, adding a pleasant scent and improving the sensory experience for users.
Used in Chemical Reactions as a Solvent:
(Benzyloxy)methanol is used as a solvent in various chemical reactions, facilitating the process and improving the efficiency of the reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 14548-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14548-60:
(7*1)+(6*4)+(5*5)+(4*4)+(3*8)+(2*6)+(1*0)=108
108 % 10 = 8
So 14548-60-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10O2/c9-7-10-6-8-4-2-1-3-5-8/h1-5,9H,6-7H2
14548-60-8Relevant articles and documents
Lewis Base–Br?nsted Acid–Enzyme Catalysis in Enantioselective Multistep One-Pot Syntheses
Giesler, Markus,Guder, Marian,Hartmann, Laura,Mantel, Marvin,Pietruszka, J?rg,Rüthlein, Elisabeth
supporting information, p. 16700 - 16706 (2021/05/07)
Establishing one-pot, multi-step protocols combining different types of catalysts is one important goal for increasing efficiency in modern organic synthesis. In particular, the high potential of biocatalysts still needs to be harvested. Based on an in-depth mechanistic investigation of a new organocatalytic protocol employing two catalysts {1,4-diazabicyclo[2.2.2]octane (DABCO); benzoic acid (BzOH)}, a sequence was established providing starting materials for enzymatic refinement (ene reductase; alcohol dehydrogenase): A gram-scale access to a variety of enantiopure key building blocks for natural product syntheses was enabled utilizing up to six catalytic steps within the same reaction vessel.
