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1679-07-8

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1679-07-8 Usage

Description

Cyclopentanethiol is a colorless liquid with a strong, alliaceous odor reminiscent of onion, garlic, horseradish, meat, egg, and burned vegetables. It is known for its unique taste characteristics, which can be detected even at a concentration of 2 ppm. Due to its distinctive flavor profile, Cyclopentanethiol is utilized in various applications across different industries.

Uses

Used in Food Industry:
Cyclopentanethiol is used as a food spice to impart a rich, savory taste to various dishes. Its ability to evoke flavors reminiscent of onion, garlic, and other vegetables makes it a valuable ingredient in enhancing the taste and aroma of food products.
Used in Pharmaceutical Industry:
Cyclopentanethiol serves as a pharmaceutical intermediate, playing a crucial role in the synthesis of various drugs and medications. Its unique chemical properties make it a versatile building block for developing new pharmaceutical compounds.
In terms of environmental impact, the annual production of Cyclopentanethiol is relatively low, at less than 1.00 lb, indicating that its use is highly specialized and controlled. This ensures that the application of Cyclopentanethiol remains focused on its specific functions in the food and pharmaceutical industries, without causing significant environmental concerns.

Preparation

From cyclopentyl bromide and potassium hydrosulfide; by treating cycloalkanone dimethyl dithioacetals with four equivalents of an alkaline metal; from cyclopentyl naphthyl sulfide and an aluminosilicate catalyst.

Safety Profile

A human poison. A flammable liquid. When heated to decomposition it emits toxic vapors of SOx

Check Digit Verification of cas no

The CAS Registry Mumber 1679-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1679-07:
(6*1)+(5*6)+(4*7)+(3*9)+(2*0)+(1*7)=98
98 % 10 = 8
So 1679-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H10S/c6-5-3-1-2-4-5/h5-6H,1-4H2

1679-07-8 Well-known Company Product Price

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

  • (L03577)  Cyclopentanethiol, 97%   

  • 1679-07-8

  • 5g

  • 329.0CNY

  • Detail
  • Alfa Aesar

  • (L03577)  Cyclopentanethiol, 97%   

  • 1679-07-8

  • 25g

  • 1379.0CNY

  • Detail
  • Aldrich

  • (319708)  Cyclopentanethiol  97%

  • 1679-07-8

  • 319708-5G

  • 292.50CNY

  • Detail
  • Aldrich

  • (319708)  Cyclopentanethiol  97%

  • 1679-07-8

  • 319708-25G

  • 967.59CNY

  • Detail

1679-07-8SDS

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 CYCLOPENTANETHIOL

1.2 Other means of identification

Product number -
Other names Cyclopentyl mercaptan

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:1679-07-8 SDS

1679-07-8Relevant articles and documents

Anodic activation of hydrogen sulfide in reaction with cyclopentane

Berberova,Shinkar',Smolyaninov,Abdulaeva

, p. 998 - 1000 (2015)

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Redox mediators of hydrogen sulfide oxidation in reactions with cycloalkanes

Berberova,Shinkar',Smolyaninov,Pashchenko

, p. 295 - 298 (2016/01/12)

An indirect electrochemical method for thiolation of cycloalkanes C5-C7 has been suggested. The method is based on a new approach to activation of hydrogen sulfide by redox mediators.

NONCONVENTIONAL FRIEDEL-CRAFTS CHEMISTRY III. ON THE REGIOSPECIFIC SYNTHESIS OF SPIRO-4'-ONE DERIVATIVES

El-Zohry, Maher F.

, p. 311 - 320 (2007/10/02)

The rection of 1-oxa-4-thiaspirononan-2-one (4) and/or 1-oxa-4-thiaspirodecan-2-one (5) with arenes (6) under the catalytic action of aluminum chloride afforded in all cases spiro-4'-ones (7a - g and 8a - g), -acetic acid, (9a - g and 10a - g), cycloalkylthioacetic acids, (11 and 20) aryl cycloalkyl sulfides, (14 and 23) diarylsulfides (15), diaryl disulfides and dicycloalkyl disulfides (13 and 22).The mechanisms of these reactions are discussed.Key words: Spiroisothiochroman-4-ones; Friedel-Crafts reactions.

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