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2-Butanone, 4-(2-methyl-1H-indol-3-yl)-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97355-53-8 Structure
  • Basic information

    1. Product Name: 2-Butanone, 4-(2-methyl-1H-indol-3-yl)-4-phenyl-
    2. Synonyms:
    3. CAS NO:97355-53-8
    4. Molecular Formula: C19H19NO
    5. Molecular Weight: 277.366
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97355-53-8.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: 2-Butanone, 4-(2-methyl-1H-indol-3-yl)-4-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butanone, 4-(2-methyl-1H-indol-3-yl)-4-phenyl-(97355-53-8)
    11. EPA Substance Registry System: 2-Butanone, 4-(2-methyl-1H-indol-3-yl)-4-phenyl-(97355-53-8)
  • 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: 97355-53-8(Hazardous Substances Data)

97355-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97355-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,5 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97355-53:
(7*9)+(6*7)+(5*3)+(4*5)+(3*5)+(2*5)+(1*3)=168
168 % 10 = 8
So 97355-53-8 is a valid CAS Registry Number.

97355-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-methyl-1H-indol-3-yl)-4-phenylbutan-2-one

1.2 Other means of identification

Product number -
Other names 4-(2-methyl-indol-3-yl)-4-phenyl-butan-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:97355-53-8 SDS

97355-53-8Downstream Products

97355-53-8Relevant articles and documents

Air-stable μ2-hydroxyl bridged cationic binuclear complexes of zirconocene perfluorooctanesulfonates: their structures, characterization and application

Zhang, Xiaohong,Xu, Xinhua,Li, Ningbo,Liang, Zhiwu,Tang, Zilong

supporting information, p. 1926 - 1932 (2018/03/21)

Three air-stable zirconocene perfluoro-octanesulfonates were successfully synthesized by treatment of C8F17SO3Ag with (RCp)2ZrCl2 [R = H, n-Bu, t-Bu]. According to X-ray analysis, they have μ2-hydroxyl bridged cationic binuclear structures: (i) [CpZr(OH2)3]2(μ2-OH)2(OSO2C8F17)4·2THF·4H2O (1a·2THF·4H2O), (ii) [n-BuCpZr(OH2)3]2(μ2-OH)2(OSO2C8F17)4·6H2O (2a·6H2O), and (iii) [t-BuCpZr(OH2)3]2(μ2-OH)2(OSO2C8F17)4·2C3H6O·8H2O (3a·2C3H6O·8H2O). The ligands of water and organic molecules in the complexes originated from the moist air and solvent during their recrystallization. These complexes were characterized with different techniques, and found to show water tolerance, air/thermal stability as well as strong Lewis acidity. Moreover, the complexes showed highly catalytic activity in various reactions of C–C bond formation. With good recyclability, they should find wide applications in organic chemistry.

Supported iron catalysts for Michael addition reactions

Ye, Rong,Faucher, Franco F.,Somorjai, Gabor A.

, p. 65 - 71 (2018/02/13)

Heterogeneous catalysts have been widely used for chemical transformations and offer easy product separation in addition to their high activity. Iron is an earth-abundant metal, but it has not been studied thoroughly as heterogeneous catalysts for organic

Sulfonic acid-functionalized magnetic nanoparticles as a recyclable and eco-friendly catalyst for atom economical Michael addition reactions and bis indolyl methane synthesis

Mahmoudi, Hajar,Jafari, Abbas Ali,Saeedi, Soroosh,Firouzabadi, Habib

, p. 3023 - 3030 (2015/02/05)

A modified sulfonic acid functionalized magnetic nanoparticle composite (Fe3O4@γFe2O3-SO3H) is prepared by the use of ultrasonic irradiation. By this modification, the size of the nano-particles was r

From waste biomass to solid support: Lignosulfonate as a cost- Effective and renewable supporting material for catalysis

Sun, Shaohuan,Bai, Rongxian,Gu, Yanlong

supporting information, p. 549 - 558 (2014/04/03)

Lignosulfonate (LS) is an organic waste generated as a byproduct of the cooking process in sulfite pulping in the manufacture of paper. In this paper, LS was used as an anionic supporting material for immobilizing cationic species, which can then be used as heterogeneous catalysts in some organic transformations. With this strategy, three lignin-supported catalysts were prepared including 1) lignin- SO3Sc(OTf)2, 2) lignin-SO3Cu(OTf), and 3) lignin-IL@NH2 (IL= ionic liquid). These solid materials were then examined in many organic transformations. It was finally found that, compared with its homogeneous counterpart as well as some other solid catalysts that are prepared by using different supports with the same metal or catalytically active species, the lignin-supported catalysts showed better performance in these reactions not only in terms of activity but also with regard to recyclability.

Gluconic acid aqueous solution as a sustainable and recyclable promoting medium for organic reactions

Zhou, Binghua,Yang, Jie,Li, Minghao,Gu, Yanlong

supporting information; experimental part, p. 2204 - 2211 (2011/10/03)

For the first time, gluconic acid aqueous solution (GAAS), a biobased weakly acidic liquid, was used as an effective promoting medium for organic reactions, such as the Michael addition of indoles to α,β-unsaturated ketones, the electrophilic ring-opening

Sulfamic acid as a cost-effective and recyclable solid acid catalyst for Friedel-Crafts alkylation of indole with α,β-unsaturated carbonyl compound and benzyl alcohol

Yang, Jing,Zhang, Juan,Chen, Tian Tian,Sun, De Mei,Li, Ji,Wu, Xue Fen

experimental part, p. 1391 - 1394 (2012/06/01)

Sulfamic acid was proved to be a cost-effective and recyclable catalyst for Friedel-Crafts type reaction of indole with α,β-unsaturated carbonyl compound and benzyl alcohol. Various indoles, α,β-unsaturated carbonyl compounds and a benzyl alcohol were suc

Zirconium tetrakis(dodecylsulfate) as an efficient and recyclable lewis acid-surfactant-combined catalyzed C-C and C-N bond forming under mild and environmentally benign conditions

Jafarpour, Maasoumeh,Rezaeifard, Abdolreza,Aliabadi, Marzieh

scheme or table, p. 94 - 99 (2010/04/23)

A green catalytic method for C-C and C-N bond forming via Michael addition of aromatic amines and indoles to electron-deficient olefins using Zirconium tetrakis(dodecylsulfate) in water under mild conditions with high yields and selectivity has been developed. The reusability of the catalyst has been successfully examined without any noticeable loss of its catalytic activity.

Antimony(III) sulfate catalyzed condensation reaction of indoles with carbonyl compounds

Srinivasa, Aswathanarayana,Varma, Putta Prabhakar,Hulikal, Vijaykumar,Mahadevan, Kittappa M.

, p. 111 - 115 (2008/09/21)

Antimony sulfate was found to be on effective catalyst for the condensation reaction of indoles with carbonyl compounds at room temperature. This catalyst is inexpensive, easily available and it was also found that this catalyst could be recovered quantitatively and reused without much loss of catalytic activity.

Synthesis of 3-substituted indoles promoted by pulverization-activation method catalyzed by Bi(NO3)3·5H2O

Khodaei, Mohammad M.,Mohammadpoor-Baltork, Iraj,Memarian, Hamid R.,Khosropour, Ahmad R.,Nikoofar, Kobra,Ghanbary, Parvin

, p. 377 - 381 (2008/09/20)

(Chemical Equation Presented) A new, facile, efficient, "green" and chemoselective procedure for the synthesis of indole derivatives has been developed with pulverization-activation method catalyzed by Bi(NO 3)3·5H2O (PAMC- Bi(NO3) 3·5H2O) through grinding of indoles with aldehydes or Michael acceptors in the presence of catalytic amounts of Bi(NO 3)3·5H2O under solvent-free conditions.

Triflic acid-catalyzed Michael reactions of indole and pyrrole compounds with α,β-unsaturated ketones in water

Zhang, Hai-Bo,Liu, Li,Liu, Yu-Liang,Chen, Yong-Jun,Wang, Jun,Wang, Dong

, p. 173 - 181 (2007/10/03)

The Michael reactions of indole and pyrrole compounds to α,β-unsaturated ketones catalyzed by triflic acid (HOTf, 0.1-1 mol%) were performed in water to give alkylated indoles (3a-m) and dialkylsubstituted pyrroles (6a-b) in good to excellent yields. Copy

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