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Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 424788-79-4 Structure
  • Basic information

    1. Product Name: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester
    2. Synonyms:
    3. CAS NO:424788-79-4
    4. Molecular Formula: C9H7F3O5S
    5. Molecular Weight: 284.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 424788-79-4.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: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(424788-79-4)
    11. EPA Substance Registry System: Methanesulfonic acid, trifluoro-, 2-formyl-4-methoxyphenyl ester(424788-79-4)
  • 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: 424788-79-4(Hazardous Substances Data)

424788-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 424788-79-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,4,7,8 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 424788-79:
(8*4)+(7*2)+(6*4)+(5*7)+(4*8)+(3*8)+(2*7)+(1*9)=184
184 % 10 = 4
So 424788-79-4 is a valid CAS Registry Number.

424788-79-4SDS

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 (2-formyl-4-methoxyphenyl) trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names 2-formyl-4-methoxyphenyltrifluoromethanesulfonate

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:424788-79-4 SDS

424788-79-4Relevant articles and documents

CYCLOPROPYL ETHYLENE COMPOUND AND ARTHROPOD PEST CONTROL COMPOSITION CONTAINING SAME

-

Paragraph 0321-0322, (2021/02/05)

The present invention provides a compound that have excellent harmful arthropod controlling effects, the compounds being represented by formula (I) [wherein R1 represents a hydrogen atom etc., and R21, R22, R31

Construction of spirofused tricyclic frameworks by NHC-catalyzed intramolecular stetter reaction of a benzaldehyde tether with a cyclic exsnone

Hsu, Day-Shin,Cheng, Chiao-Yun

, p. 10832 - 10842 (2019/09/30)

Various benzaldehyde tethers with a cyclic enone were prepared from commercially available 2-hydroxybenzaldehydes via a three-step sequence involving triflate formation, Sonogashira cross-coupling, and regioselective hydrogenation. These substrates were t

[...] compound pest control method (by machine translation)

-

Paragraph 0239, (2020/01/02)

[A] a method for controlling harmful organisms. (I) formula [a][In the formula, R1 The, represents a hydrogen atom or the like, R21 , R22 , R31 , And R32 The, same or different, represents a hydrogen

Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids

Si, Tengda,Li, Bowen,Xiong, Wenrui,Xu, Bin,Tang, Wenjun

supporting information, p. 9903 - 9909 (2017/12/12)

Aryl-secondary alkyl cross-coupling with aryl sulfonate esters as coupling partners remains a significant challenge. Efficient cross-coupling between aryl/alkenyl triflates and acyclic secondary alkylboronic acids is realized for the first time to provide a series of sterically congested acyclic secondary alkyl arenes/olefins in good to excellent yields. The employment of sterically bulky P,PO ligand L1/L2 is crucial for the high yields and selectivities. The method has enabled a concise and 4-step synthesis of a key intermediate of male contraceptive agent and PAF antagonist gossypol.

Pd(II)-catalyzed one-pot, three-step route for the synthesis of unsymmetrical acridines

Guo, Hai-Ming,Mao, Run-Ze,Wang, Qiao-Tian,Niu, Hong-Ying,Xie, Ming-Sheng,Qu, Gui-Rong

supporting information, p. 5460 - 5463 (2013/11/19)

Unsymmetric acridines are synthesized via a one-pot amination/cyclization/ aromatization reaction for the first time. With Pd(OAc)2-X-Phos as the catalyst, a series of unsymmetric acridines are obtained in moderate to excellent yields (up to 99

COMPOUNDS ACT AT MULTIPLE PROSTAGLANDIN RECEPTORS GIVING A GENERAL ANTI-INFLAMMATORY RESPONSE

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Page/Page column 16, (2012/03/11)

The present invention provides compounds, that areN-alkyl-2-(l-(5-substituted-2-(3- oxo-3-(trifluoromethylsulfonamido)propyl)benzyl)pyrrolidin-2-yl)oxazole-4-carboxamide wherein the 5 substituent is selected from the group consisting of halo and alkyloxy

FATTY ACID AMIDE HYDROLASE INHIHIBITORS FOR TREATING PAIN

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Page/Page column 9, (2012/11/07)

Compounds of Formula 1 are described herein. These compounds may be administered to a patient for treatment of suffering from pain or other FAAH mediated conditions.

Synthesis and biological evaluations of P4-benzoxaborole-substituted macrocyclic inhibitors of HCV NS3 protease

Ding, Charles Z.,Zhang, Yong-Kang,Li, Xianfeng,Liu, Yang,Zhang, Suoming,Zhou, Yasheen,Plattner, Jacob J.,Baker, Stephen J.,Liu, Liang,Duan, Maosheng,Jarvest, Richard L.,Ji, Jingjing,Kazmierski, Wieslaw M.,Tallant, Matthew D.,Wright, Lois L.,Smith, Gary K.,Crosby, Renae M.,Wang, Amy A.,Ni, Zhi-Jie,Zou, Wuxin,Wright, Jon

scheme or table, p. 7317 - 7322 (2011/01/12)

We disclose here a series of P4-benzoxaborole-substituted macrocyclic HCV protease inhibitors. These inhibitors are potent against HCV NS3 protease, their anti-HCV replicon potencies are largely impacted by substitutions on benzoxaborole ring system and P2 groups. P2 2-thiazole-isoquinoline provides best replicon potency. The in vitro SAR studies and in vivo PK evaluations of selected compounds are described herein.

Oxaziridine-mediated intramolecular amination of sp3-hybridized c-h bonds

Allen, Charles P.,Benkovics, Tamas,Turek, Amanda K.,Yoon, Tehshik P.

supporting information; experimental part, p. 12560 - 12561 (2010/01/29)

(Chemical Equation Presented) We describe a new oxaziridine-mediated approach to the amination of sp3-hybridized C-H bonds. In the presence of a copper(II) catalyst, N-sulfonyl oxaziridines participate in efficient intramolecular cyclization re

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