85902-68-7 Usage
Uses
Used in Fragrance and Flavor Industry:
5-ISOPROPYL-2-METHOXYBENZALDEHYDE is used as a key ingredient in the fragrance and flavor industry for its pleasant aroma, enhancing the sensory experience of various products.
Used in Pharmaceutical Synthesis:
5-ISOPROPYL-2-METHOXYBENZALDEHYDE is used as a raw material for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Agrochemical Synthesis:
In the agrochemical industry, 5-ISOPROPYL-2-METHOXYBENZALDEHYDE is utilized as a starting material for the production of different agrochemicals, supporting agricultural productivity and pest management.
Used in Material Development:
5-ISOPROPYL-2-METHOXYBENZALDEHYDE has potential applications in the development of new materials, indicating its versatility and importance in the field of material science.
Used in Chemical Research:
5-ISOPROPYL-2-METHOXYBENZALDEHYDE is also used in chemical research, where it may serve as a precursor or intermediate in various chemical reactions, aiding in the advancement of scientific knowledge and innovation.
It is crucial to handle 5-ISOPROPYL-2-METHOXYBENZALDEHYDE with care, as it may cause irritation to the skin, eyes, and respiratory system, highlighting the need for proper safety measures during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 85902-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85902-68:
(7*8)+(6*5)+(5*9)+(4*0)+(3*2)+(2*6)+(1*8)=157
157 % 10 = 7
So 85902-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O2/c1-8(2)9-4-5-11(13-3)10(6-9)7-12/h4-8H,1-3H3
85902-68-7Relevant academic research and scientific papers
Formylation process for aromatic aldehydes
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, (2008/06/13)
A novel two-step reaction process for preparing 5-substituted-2-methoxybenzaldehyde compounds is disclosed wherein the substituent group is either isopropyl or trifluoromethoxy. The process involves (1) reacting a corresponding 4-substituted phenol compou
