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113093-83-7

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113093-83-7 Usage

Molecular structure

1-Propanone backbone with an ethylthio group (-C2H5SH) attached to the second carbon, a hydroxyphenyl group (-C6H4OH) attached to the first carbon, and a phenyl group (-C6H5) attached to the third carbon.

Complexity

The compound has a complex structure with multiple functional groups.

Usage

Commonly used in organic synthesis and pharmaceutical research.

Biological activity

Potential antifungal and anti-tumor properties, and has been studied for its potential use in the development of new drugs and therapeutic agents.

Further research

More research is needed to fully understand its potential applications and biological effects.

Check Digit Verification of cas no

The CAS Registry Mumber 113093-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,9 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113093-83:
(8*1)+(7*1)+(6*3)+(5*0)+(4*9)+(3*3)+(2*8)+(1*3)=97
97 % 10 = 7
So 113093-83-7 is a valid CAS Registry Number.

113093-83-7SDS

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 2-ethylsulfanyl-1-(2-hydroxyphenyl)-3-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 1-(2-Hydroxyphenyl)-2-ethylthio-3-phenyl-propan-1-one

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:113093-83-7 SDS

113093-83-7Relevant articles and documents

FLAVONOIDS, 40. SYNTHESIS OF 3-ALKYL- AND -ARYLTHIOFLAVANONES AND THEIR TRANSFORMATIONS INTO SULFUR-CONTAINING FLAVONOIDS

Patonay, Tamas,Patonay-Peli, Erzsebet,Litkei, Gyoergy

, p. 1827 - 1834 (2007/10/02)

trans-3-Mesyloxyflavanones 1 were converted into cis- and trans-3-(alkylthio)- and -(phenylthio)flavanones 2-4 by nucleophilic substitution reaction with thiols or thiolates.Flavanones 2-4 were useful intermediates in the synthesis of various sulfur-containing derivatives; flavanones, flavones and dihydrochalcones posessing alkyl- or arylthio, -sulfinyl and -sulfonyl group.Oxidation of cis- and trans- isomers of 4 led to completely different products.

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