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22002-73-9

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22002-73-9 Usage

General Description

3-(n-Butylsulphanyl)propionic acid is a chemical compound with the molecular formula C8H16O2S2. It is a derivative of propionic acid, with a butylsulphanyl group attached to the third carbon atom. 3-(n-Butylsulphanyl)propionic acid is commonly used as a building block in organic synthesis and has potential applications in the pharmaceutical and agrochemical industries. It may also be used as a reagent in chemical reactions, particularly in the formation of carbon-carbon and carbon-sulfur bonds. Its properties and reactivity make it a versatile compound with various potential uses in different fields of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 22002-73-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,0 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22002-73:
(7*2)+(6*2)+(5*0)+(4*0)+(3*2)+(2*7)+(1*3)=49
49 % 10 = 9
So 22002-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O2S/c1-2-3-5-10-6-4-7(8)9/h2-6H2,1H3,(H,8,9)

22002-73-9SDS

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 3-butylsulfanylpropanoic acid

1.2 Other means of identification

Product number -
Other names Propionic acid,3-(butylthio)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:22002-73-9 SDS

22002-73-9Relevant articles and documents

An improved and green preparation of 3-(alkylthio)propionic acids

Vaismaa, Matti J. P.,Yliniemel?, Sanna M.,Lajunen, Marja K.

, p. 1317 - 1323 (2008/10/09)

An efficient, facile microwave-assisted synthesis has been developed for the preparation of unsymmetrical sulfide derivatives from 3-mercaptopropionic acid and a wide variety of alkyl, allyl or aryl chlorides or bromides. The synthesis performed in ethanol at 80 or 120 °C using sodium hydroxide as a base, selectively without an offensive smell, generates 3-(alkylthio)propionic acids in good yields. Effects of reaction components, temperature, and the heating technique on the formation of the product and side-products were studied.

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