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2(3H)-Furanone, dihydro-5-[(4-methylphenyl)thio]-4-(2-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

596119-48-1

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596119-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 596119-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 596119-48:
(8*5)+(7*9)+(6*6)+(5*1)+(4*1)+(3*9)+(2*4)+(1*8)=191
191 % 10 = 1
So 596119-48-1 is a valid CAS Registry Number.

596119-48-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methylphenyl)sulfanyl-4-(2-phenylethyl)oxolan-2-one

1.2 Other means of identification

Product number -
Other names 4-(2-phenylethyl)-5-(p-tolylsulfanyl)-4,5-dihydro-3H-furan-2-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:596119-48-1 SDS

596119-48-1Relevant articles and documents

A new synthesis of amides and γ-lactones based on the conjugate addition of lithium enolate of amides to 1-chlorovinyl p-tolyl sulfoxides

Satoh, Tsuyoshi,Kamide, Yuhki,Sugiyama, Shimpei

, p. 11805 - 11812 (2007/10/03)

Reaction of 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from chloromethyl p-tolyl sulfoxide and ketones or aldehydes, with lithium enolate of N,N-dimethylacetamide gave the adducts in good to quantitative yields. The adducts were converted to

Conjugate addition of lithium ester enolates to 1-chlorovinyl p-tolyl sulfoxides: A novel synthesis of functionalized esters and lactones having a tertiary or a quaternary carbon at the β-position

Satoh, Tsuyoshi,Sugiyama, Shimpei,Kamide, Yuhki,Ota, Hiroyuki

, p. 4327 - 4336 (2007/10/03)

Addition of the lithium ester enolates to 1-chlorovinyl p-tolyl sulfoxides, which were synthesized from chloromethyl p-tolyl sulfoxide and ketones or aldehydes, gave esters having a tertiary or a quaternary carbon at the 3-position, and chlorine and sulfi

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