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4-(ETHYLTHIO)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84211-94-9

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84211-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84211-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,1 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84211-94:
(7*8)+(6*4)+(5*2)+(4*1)+(3*1)+(2*9)+(1*4)=119
119 % 10 = 9
So 84211-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H10OS/c1-2-11-9-5-3-8(7-10)4-6-9/h3-7H,2H2,1H3

84211-94-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L17624)  4-(Ethylthio)benzaldehyde, 98%   

  • 84211-94-9

  • 1g

  • 429.0CNY

  • Detail
  • Alfa Aesar

  • (L17624)  4-(Ethylthio)benzaldehyde, 98%   

  • 84211-94-9

  • 5g

  • 1645.0CNY

  • Detail

84211-94-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethylsulfanylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-ethylthiobenzaldehyde

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:84211-94-9 SDS

84211-94-9Relevant academic research and scientific papers

β-Lactam analogues of combretastatin A-4 prevent metabolic inactivation by glucuronidation in chemoresistant HT-29 colon cancer cells

Malebari, Azizah M.,Greene, Lisa M.,Nathwani, Seema M.,Fayne, Darren,O'Boyle, Niamh M.,Wang, Shu,Twamley, Brendan,Zisterer, Daniela M.,Meegan, Mary J.

, p. 261 - 285 (2017/03/09)

Glucuronidation by uridine 5-diphosphoglucuronosyl transferase enzymes (UGTs) is a cause of intrinsic drug resistance in cancer cells. Glucuronidation of combretastatin A-4 (CA-4) was previously identified as a mechanism of resistance in hepatocellular ca

COMPOUNDS FOR TREATING MUSCULAR DYSTROPHY

-

Page/Page column 53, (2010/12/29)

Compounds of formula (I): wherein X, L1, R1, L2, R2, R3, and R4 are as defined herein, are useful in the treatment or prophylaxis of Duchenne muscular dystrophy, Becker muscular dystrophy, or cachexia.

Synthesis and serotonin transporter activity of sulphur-substituted α-alkyl phenethylamines as a new class of anticancer agents

Cloonan, Suzanne M.,Keating, John J.,Butler, Stephen G.,Knox, Andrew J.S.,Jorgensen, Anne M.,Peters, Guenther H.,Rai, Dilip,Corrigan, Desmond,Lloyd, David G.,Williams, D. Clive,Meegan, Mary J.

scheme or table, p. 4862 - 4888 (2010/01/16)

The discovery that some serotonin reuptake transporter (SERT) ligands have the potential to act as pro-apoptotic agents in the treatment of cancer adds greatly to their diverse pharmacological application. 4-Methylthioamphetamine (MTA) is a selective ligand for SERT over other monoamine transporters. In this study, a novel library of structurally diverse 4-MTA analogues were synthesised with or without N-alkyl and/or C-α methyl or ethyl groups so that their potential SERT-dependent antiproliferative activity could be assessed. Many of the compounds displayed SERT-binding activity as well as cytotoxic activity. While there was no direct correlation between these two effects, a number of derivatives displayed anti-tumour effects in lymphoma, leukaemia and breast cancer cell lines, showing further potential to be developed as possible chemotherapeutic agents.

NOVEL IMIDAZOLES WITH ANTI-INFLAMMATORY ACTIVITY

-

, (2008/06/13)

Compounds of formula I wherein: one of X or Y represents N and the other represents C; R1 represents hydrogen, methyl, halogen, cyano, nitro, -CHO, -COCH3 or -COOR4; R2 represents optionally-substituted aryl or heteroaryl; R3 represents C1-8 alkyl, C1-8 haloalkyl or -NR4R6; R4 represents hydrogen, C1-8 alkyl or arylC0-8 alkyl; R6 represents hydrogen, C1-8 alkyl, arylC1-8 alkyl, -COR8 or -COOR8; R8 represents C1-8 alkyl or C1-8 haloalkyl; aryl in the above definitions represents phenyl or naphthyl; and heteroaryl in the above definitions represents pyridine, pyrazine, pyrimidine or pyridazine, which can be optionally fused to a benzene ring. These compounds are useful as cyclooxygenase-2 inhibitors.

Reaction of Styrene 3,4-Oxide with Ethanediol and Dehydration to Ethylthiostyrenes

Watabe, Tadashi,Hiratsuka, Akira,Sone, Tomomichi,Ishihama, Tetsuya

, p. 585 - 586 (2007/10/02)

Styrene 3,4-oxide reacts with the nucleophile ethanediol, and the product is dehydrated to give three isomeric ethylthiostyrenes via the corresponding ethylthiovinylcyclohexadienols without formation of thiiranium ions as intermediates.

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