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20600-63-9

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20600-63-9 Usage

General Description

ALLYLSULFANYL-ACETIC ACID is a chemical compound that is classified as an organic compound and a sulfur compound. It consists of an allyl group attached to a sulfanyl group and an acetic acid group. It is commonly used in the production of pharmaceuticals and is known for its potential anti-cancer properties. Research has also shown that it may have anti-inflammatory and antioxidant effects. Additionally, it is used in the synthesis of various organic compounds and as a building block for the creation of other chemical compounds. Overall, ALLYLSULFANYL-ACETIC ACID has a range of potential applications in the fields of medicine and chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 20600-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,0 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20600-63:
(7*2)+(6*0)+(5*6)+(4*0)+(3*0)+(2*6)+(1*3)=59
59 % 10 = 9
So 20600-63-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2S/c1-2-3-8-4-5(6)7/h2H,1,3-4H2,(H,6,7)

20600-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enylsulfanylacetic acid

1.2 Other means of identification

Product number -
Other names Allylmercapto-essigsaeure

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:20600-63-9 SDS

20600-63-9Relevant articles and documents

Dicobalt hexacarbonyl complexes of alkynyl imines in a sequential Staudinger/Pauson-Khand process. A route to new fused tricyclic β-lactams

Olier, Clarisse,Azzi, Nadia,Gil, Gerard,Gastaldi, Stephane,Bertrand, Michele P.

supporting information; experimental part, p. 8469 - 8473 (2009/04/11)

(Chemical Equation Presented) Dicobalt hexacarbonyl complexes of alkynyl imines were allowed to react with ketenes via Staudinger reaction. Sequential [2 + 2] cycloaddition/Pauson-Khand reaction led to structurally new fused-tricyclic β-lactams and fused-

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