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1759-28-0

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1759-28-0 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 1759-28-0 differently. You can refer to the following data:
1. CLEAR YELLOW TO BROWN LIQUID
2. 4-Methyl-5-vinylthiazole has a nutty, cocoa odor.

Occurrence

Reported found in cocoa aroma, yellow passion fruit aroma, garlic, pork, cognac, roasted filberts and soursop.

Uses

4-Methyl-5-vinylthiazole is found in flowers and is highly attractive to both male and female beetles of three species of the genus Cyclocephala, pollinators of the studied plant taxa.

Taste threshold values

Taste characteristics at 20 ppm: nutty, musty, earthy, cocoa powder-like

General Description

4-Methyl-5-vinylthiazole is a nitrogen and sulphur-containing heterocyclic compound, present in the species of Annona (magnoliids, Annonaceae) and Caladium bicolor (monocots, Araceae). It is extremely attractive to both male and female beetles of three species of the genus Cyclocephala.

Check Digit Verification of cas no

The CAS Registry Mumber 1759-28-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1759-28:
(6*1)+(5*7)+(4*5)+(3*9)+(2*2)+(1*8)=100
100 % 10 = 0
So 1759-28-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NS/c1-3-6-5(2)7-4-8-6/h3-4H,1H2,2H3

1759-28-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B21719)  4-Methyl-5-vinylthiazole, 98+%   

  • 1759-28-0

  • 5g

  • 413.0CNY

  • Detail
  • Alfa Aesar

  • (B21719)  4-Methyl-5-vinylthiazole, 98+%   

  • 1759-28-0

  • 25g

  • 1410.0CNY

  • Detail
  • Alfa Aesar

  • (B21719)  4-Methyl-5-vinylthiazole, 98+%   

  • 1759-28-0

  • 100g

  • 5345.0CNY

  • Detail
  • Aldrich

  • (242004)  4-Methyl-5-vinylthiazole  99%

  • 1759-28-0

  • 242004-5G

  • 374.40CNY

  • Detail

1759-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methyl-5-vinylthiazole

1.2 Other means of identification

Product number -
Other names Vinylsulfurol

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:1759-28-0 SDS

1759-28-0Relevant articles and documents

PyFluor: A low-cost, stable, and selective deoxyfluorination reagent

Nielsen, Matthew K.,Ugaz, Christian R.,Li, Wenping,Doyle, Abigail G.

supporting information, p. 9571 - 9574 (2015/08/18)

We report an inexpensive, thermally stable deoxyfluorination reagent that fluorinates a broad range of alcohols without substantial formation of elimination side products. This combination of selectivity, safety, and economic viability enables deoxyfluorination on preparatory scale. We employ the [18F]-labeled reagent in the first example of a no-carrier-added deoxy-radiofluorination.

Concise synthesis of vinylheterocycles through β-elimination under solventless phase transfer catalysis conditions

Albanese, Domenico,Ghidoli, Cristina,Zenoni, Maurizio

, p. 736 - 739 (2013/01/03)

Various vinylheterocycles compounds have been prepared in excellent yields through β-elimination of the corresponding sulfonate esters with 50% aq NaOH under phase transfer catalysis conditions without organic solvent. The new approach provides an economic and environmentally friendly solution to removal of hazardous bases as well as toxic and expensive dipolar aprotic solvents.

Method for treating glaucoma IIB

-

, (2008/06/13)

Provided is a method of decreasing intraocular pressure or improving ocular accommodation in an animal, including a human, comprising administering an intraocular pressure decreasing amount or ocular accommodation improving amount of a compound of the formula I or IA, wherein J is oxygen, sulfur, or N—Rd.

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