Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1-methyl-4-[(1Z)-2-[(phenylmethyl)thio]ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

334969-15-2

Post Buying Request

334969-15-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

334969-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 334969-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,9,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 334969-15:
(8*3)+(7*3)+(6*4)+(5*9)+(4*6)+(3*9)+(2*1)+(1*5)=172
172 % 10 = 2
So 334969-15-2 is a valid CAS Registry Number.

334969-15-2Downstream Products

334969-15-2Relevant academic research and scientific papers

Decarbonylation of Salicylaldehyde Activated by p-Cymene Ruthenium(II) Dimer: Implication for Catalytic Alkyne Hydrothiolation

Modem, Sarangapani,Kankala, Shravankumar,Balaboina, Ramesh,Thirukovela, Narasimha Swamy,Jonnalagadda, Sreekantha B.,Vadde, Ravinder,Vasam, Chandra Sekhar

, p. 4635 - 4642 (2016/09/28)

A stoichiometric C–H activation/decarbonylation of salicylaldehyde by [(η6-p-cymene)RuCl2]2gave a carbonyl derivative [(η6-p-cymene)RuCl(CO)(Ph-O)] (1) without the use of CO gas. A variety of polar phosphines were then incorporated into compound 1 to give new RuIIcationic catalysts, [(η6-p-cymene)Ru(CO)(Ph-O)L]BF4(2–8). These were used to catalyse the hydrothiolation of alkynes with a range of thiols in aqueous THF to give anti-Markovnikov E-linear vinyl sulfides in high yields.

One-pot synthesis of alkyl styryl sulfides free from transition metal/ligand catalyst and thiols

Heredia, Adrian A.,Penenory, Alicia B.

, p. 991 - 997 (2013/03/14)

A new protocol for the one-pot synthesis of styryl alkyl sulfides was developed. This methodology involves the in situ generation of thiolate anions by nucleophilic substitution between potassium thioacetate and alkyl halides followed by fragmentation. Further reactions of these thiolate anions with substituted (E,Z)-β-styryl halides gave the corresponding sulfides with retention of stereochemistry in good to excellent yields. This procedure does not require a metal catalyst, it proceeds under mild conditions and in short times, and it is free from malodorous and air-sensitive alkyl thiols. Copyright

Z-styryl sulfone anticancer agents

-

, (2008/06/13)

(Z)-styryl benzylsulfones of formula I are useful as anticancer agents: wherein R1is selected from the group consisting of hydrogen, chloro and nitro; R2is selected from the group consisting of hydrogen, lower alkyl, lower alkoxy, ch

Z-styryl sulfone anticancer agents

-

, (2008/06/13)

(Z)-styryl benzylsulfones of formula I are useful as anticancer agents: wherein R1is selected from the group consisting of hydrogen, chloro and nitro; R2is selected from the group consisting of hydrogen, lower alkyl, lower alkoxy, ch

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 334969-15-2