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3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 315242-23-0 Structure
  • Basic information

    1. Product Name: 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one
    2. Synonyms: 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one;3-(4-Methoxy-phenyl)-1-phenyl-3-(toluene-4-sulfonyl)-propan-1-one
    3. CAS NO:315242-23-0
    4. Molecular Formula: C23H22O4S
    5. Molecular Weight: 394.48338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 315242-23-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one(315242-23-0)
    11. EPA Substance Registry System: 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one(315242-23-0)
  • 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: 315242-23-0(Hazardous Substances Data)

315242-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315242-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,2,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 315242-23:
(8*3)+(7*1)+(6*5)+(5*2)+(4*4)+(3*2)+(2*2)+(1*3)=100
100 % 10 = 0
So 315242-23-0 is a valid CAS Registry Number.

315242-23-0SDS

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 3-(4-methoxyphenyl)-1-phenyl-3-tosylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3-(4-Methoxy-phenyl)-1-phenyl-3-(toluene-4-sulfonyl)-propan-1-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:315242-23-0 SDS

315242-23-0Downstream Products

315242-23-0Relevant articles and documents

Catalytic arylsulfonyl radical-triggered 1,5-enyne-bicyclizations and hydrosulfonylation of α,β-conjugates

Chen, Zhen-Zhen,Liu, Shuai,Hao, Wen-Juan,Xu, Ge,Wu, Shuo,Miao, Jiao-Na,Jiang, Bo,Wang, Shu-Liang,Tu, Shu-Jiang,Li, Guigen

, p. 6654 - 6658 (2015/10/28)

A catalytic bicyclization reaction of 1,5-enynes anchored by α,β-conjugates with arylsulfonyl radicals generated in situ from sulfonyl hydrazides has been established using TBAI (20 mol%) and Cu(OAc)2 (5 mol%) as co-catalysts under convenient c

Enantioselective sulfonation of enones with sulfonyl imines by cooperative N-heterocyclic-carbene/thiourea/tertiary-amine multicatalysis

Jin, Zhichao,Xu, Jianfeng,Yang, Song,Song, Bao-An,Chi, Yonggui Robin

supporting information, p. 12354 - 12358 (2013/12/04)

Many hands make light work: In an organocatalytic asymmetric sulfonation of enones, the activation of a sulfonyl imine by an N-heterocyclic carbene (NHC) catalyst led to the release of a sulfinic anion, which underwent nucleophilic addition to the enone. The enantioselectivity of the process was controlled by a chiral thiourea/amine co-catalyst through anion recognition and hydrogen-bonding interactions. Tol=p-tolyl. Copyright

FeCl3ATMSCl: An effective catalytic system for the conjugate addition of sodium p-toluenesulfinate to αβ-enones

Sreedhar,Reddy, M. Amamath,Reddy, P. Surendra

experimental part, p. 1949 - 1952 (2009/04/10)

A new protocol for the β-sulfonation of αβ-unsaturated carbonyl compounds is described. The method employs FeCl3 as catalyst and TMSC1 as additive for conjugate addition of sodiump-toluenesulfinate to enones.

Synthesis, separation and characterisation of diastereomeric mixtures of 3-p-toluenesulfonyl-1,3-diaryl-propan-1-ols

Sayed,Wadia

, p. 362 - 364 (2007/10/03)

Four diastereomeric mixtures of 3-p-toluenesulfonyl-1, 3-diarylpropan-1-ols were prepared by the reduction of the corresponding β-sulfonyl ketones and the stereochemistry of the individual separated (HPLC) diastereomers was established on the basis of PMR data.

KINETIC STUDIES ON THE ADDITION OF p-TOLUENESULFINIC ACID TO BENZYLIDENEACETOPHENONES

Kobayashi, Michio,Miura, Asako

, p. 169 - 173 (2007/10/02)

Kinetics of the addition of p-toluenesulfinic acid to p-substituted benzylideneacetophenones has been investigated.The reaction was second order, first order each in the concentration of sulfinic acid and chalcone.Effects of the p-substituents on the reac

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