34413-35-9 Usage
Uses
Used in Flavor and Fragrance Industry:
5,6,7,8-Tetrahydroquinoxaline is used as a flavoring agent for its nutty, roasted, and toasted taste characteristics. It is added to various food products to enhance their flavor and aroma, making them more appealing to consumers.
Used in Aromatherapy:
5,6,7,8-Tetrahydroquinoxaline is used as an aroma compound in aromatherapy for its pleasant and soothing scent. It can be used in candles, incense, and essential oils to create a calming and relaxing atmosphere.
Used in Perfumery:
5,6,7,8-Tetrahydroquinoxaline is used as a fixative in perfumery to enhance the longevity and stability of fragrances. Its nutty, roasted, and toasted aroma adds depth and complexity to perfumes, making them more attractive and long-lasting.
Used in Food and Beverage Industry:
5,6,7,8-Tetrahydroquinoxaline is used as a flavor enhancer in the food and beverage industry. It can be added to a variety of products, such as snacks, baked goods, and beverages, to provide a rich and complex taste profile.
Used in Cosmetics and Personal Care Products:
5,6,7,8-Tetrahydroquinoxaline is used as a fragrance ingredient in cosmetics and personal care products, such as soaps, lotions, and perfumes. Its pleasant aroma adds a sensory experience to these products, making them more enjoyable for users.
Preparation
By condensation of alicyclic α, β-diketone with an α, β-diamine; condensation of an acyclic α, β-diamine with an α, β-dicarbonyl.
Check Digit Verification of cas no
The CAS Registry Mumber 34413-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34413-35:
(7*3)+(6*4)+(5*4)+(4*1)+(3*3)+(2*3)+(1*5)=89
89 % 10 = 9
So 34413-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2/c1-2-4-8-7(3-1)9-5-6-10-8/h5-6H,1-4H2
34413-35-9Relevant articles and documents
Cobalt-bridged secondary building units in a titanium metal-organic framework catalyze cascade reduction of N-heteroarenes
Feng, Xuanyu,Song, Yang,Chen, Justin S.,Li, Zhe,Chen, Emily Y.,Kaufmann, Michael,Wang, Cheng,Lin, Wenbin
, p. 2193 - 2198 (2019/02/20)
We report here a novel Ti3-BPDC metal-organic framework (MOF) constructed from biphenyl-4,4′-dicarboxylate (BPDC) linkers and Ti3(OH)2 secondary building units (SBUs) with permanent porosity and large 1D channels. Ti-OH groups from neighboring SBUs point toward each other with an O-O distance of 2 ?, and upon deprotonation, act as the first bidentate SBU-based ligands to support CoII-hydride species for effective cascade reduction of N-heteroarenes (such as pyridines and quinolines) via sequential dearomative hydroboration and hydrogenation, affording piperidine and 1,2,3,4-tetrahydroquinoline derivatives with excellent activity (turnover number ～ 1980) and chemoselectivity.
Gas-phase Pyrolysis of 2,3-Dihydro-1,4-diazepines: Involvement of the Saturated Portion of the Ring in Chemical Reactions and Novel cis-trans Isomerisation of a Fused Ring System
Ellis, Michael J.,Lloyd, Douglas,McNab, Hamish,Walker, Marion J.
, p. 2337 - 2338 (2007/10/02)
Flash vacuum pyrolysis of 2,3-dihydro-1,4-diazepines in the range 450-550 deg C involves interaction of the saturated portion of the molecule with the vinamidine system and causes 1,5-hydrogen shifts which have been established by deuterium labelling experiments; at higher temperatures, ring contraction occurs to give pyrazines as major products.
