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34413-35-9

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34413-35-9 Usage

Description

5,6,7,8-Tetrahydroquinoxaline is a clear, very slightly yellow liquid with a nutty, roasted, and toasted aroma. It has a taste threshold value ranging from 5 to 10 ppm, with characteristics of roasted nutty, corn and popcorn, toasted grain and corn chip, taco fatty, basmati rice, hazelnut, and roasted coffee-like. It is found in various food items such as cocoa, coffee, wheat bread, fried cured pork, pork liver, roasted filbert, roasted peanut, and roasted sesame seeds.

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

34413-35-9 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L11204)  5,6,7,8-Tetrahydroquinoxaline, 99%   

  • 34413-35-9

  • 1g

  • 244.0CNY

  • Detail
  • Alfa Aesar

  • (L11204)  5,6,7,8-Tetrahydroquinoxaline, 99%   

  • 34413-35-9

  • 5g

  • 830.0CNY

  • Detail

34413-35-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6,7,8-Tetrahydroquinoxaline

1.2 Other means of identification

Product number -
Other names EINECS 252-002-8

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34413-35-9 SDS

34413-35-9Upstream product

34413-35-9Downstream Products

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.

Easy synthesis of pyrazines double substituted at 2 and 3

Nakatani,Yanatori

, p. 1509 - 1510 (2007/10/04)

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