60082-02-2 Usage
Description
1-Methylindoline-5-carboxaldehyde 97% is a chemical compound with a strong odor, commonly used as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds. It is also known for its use as a flavor and fragrance ingredient, as well as in the production of agricultural chemicals and as a reagent in organic chemistry reactions. The 97% purity of this compound ensures its suitability for various high-quality applications.
Uses
Used in Pharmaceutical Industry:
1-Methylindoline-5-carboxaldehyde 97% is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.
Used in Dye Industry:
1-Methylindoline-5-carboxaldehyde 97% is utilized as an intermediate in the production of dyes, playing a crucial role in the creation of colorants for various applications.
Used in Flavor and Fragrance Industry:
1-Methylindoline-5-carboxaldehyde 97% is used as a flavor and fragrance ingredient, adding unique scents and tastes to various products.
Used in Agricultural Chemicals Production:
1-Methylindoline-5-carboxaldehyde 97% is employed in the production of agricultural chemicals, helping to develop effective solutions for crop protection and enhancement.
Used in Organic Chemistry as a Reagent:
1-Methylindoline-5-carboxaldehyde 97% serves as a reagent in organic chemistry reactions, facilitating important processes and transformations in the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 60082-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,8 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60082-02:
(7*6)+(6*0)+(5*0)+(4*8)+(3*2)+(2*0)+(1*2)=82
82 % 10 = 2
So 60082-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c1-11-5-4-9-6-8(7-12)2-3-10(9)11/h2-3,6-7H,4-5H2,1H3
60082-02-2Relevant articles and documents
Synthesis, Structure, and Properties of Amino-Substituted Benzhydrylium Ions – A Link between Ordinary Carbocations and Neutral Electrophiles
Mayer, Robert J.,Hampel, Nathalie,Mayer, Peter,Ofial, Armin R.,Mayr, Herbert
supporting information, p. 412 - 421 (2018/09/14)
Optimized synthetic procedures for the straightforward access to eleven amino-substituted diarylmethylium tetrafluoroborates are described. These benzhydrylium ions cover a range of seven orders of magnitude in electrophilicity and provide a link between ordinary carbocations and neutral electrophiles. Five of these highly stabilized benzhydrylium tetrafluoroborates were characterized by single-crystal X-ray crystallography. While the experimentally determined bond lengths and angles in the solid state perfectly agree with those calculated by DFT methods for the gas phase and aqueous solution, crystal packing accounts for large differences in the twist angles of the aryl groups found in the solid state as compared to calculated structures.
Efficiency of the Vilsmeier-Haack method in the synthesis of p-aminobenzaldehydes
Gawinecki, Ryszard,Andrzejak, Sylwia,Puchala, Agnieszka
, p. 455 - 460 (2007/10/03)
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