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Diphenylmethyl 4-methylbenzenesulfonate is a chemical compound with the molecular formula C20H18O3S. It is a versatile reagent in organic chemistry synthesis and serves as an intermediate in the production of various products.

5435-24-5

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5435-24-5 Usage

Uses

Used in Organic Chemistry Synthesis:
Diphenylmethyl 4-methylbenzenesulfonate is used as a reagent for its ability to participate in a wide variety of chemical reactions, making it a valuable compound in the laboratory setting.
Used in Pharmaceutical Industry:
Diphenylmethyl 4-methylbenzenesulfonate is used as a building block for the synthesis of various active pharmaceutical ingredients, contributing to the development of new medications.

Check Digit Verification of cas no

The CAS Registry Mumber 5435-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5435-24:
(6*5)+(5*4)+(4*3)+(3*5)+(2*2)+(1*4)=85
85 % 10 = 5
So 5435-24-5 is a valid CAS Registry Number.

5435-24-5SDS

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 benzhydryl 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names p-Toluol-sulfonsaeure-diphenylmethylester

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:5435-24-5 SDS

5435-24-5Relevant academic research and scientific papers

Nucleophilic Displacement at Benzhydryl Centers: Asymmetric Synthesis of 1,1-Diarylalkyl Derivatives

Bolshan, Yuri,Chen, Cheng-Yi,Chilenski, Jennifer R.,Gosselin, Francis,Mathre, David J.,O'Shea, Paul D.,Roy, Amelie,Tillyer, Richard D.

, p. 111 - 114 (2007/10/03)

(Equation presented) Activation of substituted 1,1-diarylmethanols as their corresponding toluenesulfonates and subsequent displacement with a range of carbon, nitrogen, oxygen, and sulfur nucleophiles proceeds in 81-96% yield. Enantiomerically enriched d

Synthesis and biological evaluation of tropane-like 1-{2-[bis(4-fluorophenyl)methoxy]ethyl})-4-(3-phenylpropyl)piperazine (GBR 12909) analogues

Zhang,Joseph,Bowen,Flippen-Anderson,Dersch,Rothman,Jacobson,Rice

, p. 3937 - 3945 (2007/10/03)

We have prepared azabicyclo[3.2.1] derivatives (C-3-substituted tropanes) that bind with high affinity to the dopamine transporter and inhibit dopamine reuptake. Within the series, 3-{(2-[bis-(4-fluorophenyl)methoxy] ethylidene}-8-methyl-8-azabicyclo[3.2.

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