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Acetaldehyde, [(4-methylphenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41208-03-1 Structure
  • Basic information

    1. Product Name: Acetaldehyde, [(4-methylphenyl)thio]-
    2. Synonyms:
    3. CAS NO:41208-03-1
    4. Molecular Formula: C9H10OS
    5. Molecular Weight: 166.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41208-03-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetaldehyde, [(4-methylphenyl)thio]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetaldehyde, [(4-methylphenyl)thio]-(41208-03-1)
    11. EPA Substance Registry System: Acetaldehyde, [(4-methylphenyl)thio]-(41208-03-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 41208-03-1(Hazardous Substances Data)

41208-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41208-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,0 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41208-03:
(7*4)+(6*1)+(5*2)+(4*0)+(3*8)+(2*0)+(1*3)=71
71 % 10 = 1
So 41208-03-1 is a valid CAS Registry Number.

41208-03-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylphenyl)sulfanylacetaldehyde

1.2 Other means of identification

Product number -
Other names (4-Methyl-phenyl-mercapto)-acetaldehyd

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:41208-03-1 SDS

41208-03-1Relevant articles and documents

Reactions of nitronates derived from simple nitro alkanes with some thio-stabilized cationic intermediates

Lyapkalo,Lazareva,Dil'man,Ioffe,Smit

, p. 488 - 494 (1999)

Trimethylsilyl and DBU nitronates derived from nitromethane and nitropropanes do not undergo C-alkylation by episulfonium (ESI) or thiophanium (TPI) cationic intermediates. The above-mentioned derivatives of 1-nitropropane react with ESI and TPI to give the corresponding products of O-alkylation of 1-chloro-1-oxyiminopropane. The reactions of DBU nitronates derived from nitromethane and 2-nitropropane with ESI or TPI proceed as O-alkylation followed by standard fragmentation of the initially formed nitronate intermediates to give methyl (4-tolylthio)acetate or methyl 2,2-dimethyl-3-methyloxy-(4-tolylthio)butanoate respectively.

Benzyne 1,2,4-Trisubstitution and Dearomative 1,2,4-Trifunctionalization

Chen, Zhonghong,Dai, Liang,Lan, Yu,Li, Lianggui,Li, Yang,Shan, Chunhui,Shi, Jiarong,Tan, Min

supporting information, p. 10530 - 10536 (2021/07/28)

Both 1,2,4-trisubstitution and dearomative 1,2,4-trifunctionalization of benzyne have been accomplished from sulfoxides bearing a penta-2,4-dien-1-yl moiety. These cascade transformations proceed through a benzyne insertion into the S═O bond and an uncommon regiospecific anionic [4,5]-sigmatropic rearrangement, furnishing a C-O, C-S, and C-C bond on the C1-, C2-, and C4-position of a benzene ring, respectively. This study showcases new cascade benzyne reaction modes involving both distal C-H bond functionalization and dearomatization.

2-(phenylthio)ethylidene derivatives as anti-Trypanosoma cruzi compounds: Structural design, synthesis and antiparasitic activity

Cardoso, Marcos Veríssimo de Oliveira,de Oliveira Filho, Gevanio Bezerra,de Siqueira, Lucianna Rabelo Pessoa,Espíndola, José Wanderlan Pontes,Silva, Elany Barbosa da,Mendes, Andresa Pereira de Oliveira,Pereira, Valéria Rêgo Alves,de Castro, Maria Carolina Accioly Brelaz,Ferreira, Rafaela Salgado,Villela, Filipe Silva,Costa, Francielly Morais Rodrigues da,Meira, Cássio Santana,Moreira, Diogo Rodrigo Magalh?es,Soares, Milena Botelho Pereira,Leite, Ana Cristina Lima

, p. 191 - 203 (2019/07/16)

Chagas disease is an illness caused by the protozoan parasite Trypanosoma cruzi. The current chemotherapy is based on benznidazole, and, in some countries, Nifurtimox, which is effective in the acute phase of the disease, but its efficacy in the chronic p

Synthesis, docking, and in vitro activity of thiosemicarbazones, aminoacyl-thiosemicarbazides and acyl-thiazolidones against Trypanosoma cruzi

Leite, Ana Cristina Lima,de Lima, Renata Souza,Moreira, Diogo Rodrigo de M.,Cardoso, Marcos Verissimo de O.,Gouveia de Brito, Ana Carolina,Farias dos Santos, Luciene Maria,Hernandes, Marcelo Zaldini,Kiperstok, Alice Costa,de Lima, Ricardo Santana,Soares, Milena B.P.

, p. 3749 - 3757 (2007/10/03)

A novel series of thiosemicarbazone and aminoacyl-thiazolidones derivatives were synthesized. Their structure suggests that these compounds could have anti-Trypanosoma cruzi activity. Biological evaluation indicates that some of these compounds are able t

The use of tert-Butyl vinyl ether in stepwise electrophllic addition reactions

Koikov, Leonid N.,Han, Mingming,Wellman, Dawn M.,Kelly, Jim A.,Smoliakova, Irina P.

, p. 3451 - 3464 (2007/10/03)

tert-Butyl vinyl ether (1) reacts with p-TolSCl to give 2-tert-butoxy-2-chloroethyl p-tolyl sulfide (2). In the presence of SnCl4, 2 reacts with silyl enol ethers, allyltrimethylsilane, and vinyl ethers to form a C-C bond. In the case of vinyl ethers, the reaction proceeds through the formation of the 5-membered sulfonium salt intermediate which in turn can react with H2O, TMSCN, allyltrimethylsilane, and Grignard reagents.

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