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69333-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69333-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,3,3 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69333-48:
(7*6)+(6*9)+(5*3)+(4*3)+(3*3)+(2*4)+(1*8)=148
148 % 10 = 8
So 69333-48-8 is a valid CAS Registry Number.

69333-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(benzenesulfonyl)-1-methoxyethyl]benzene

1.2 Other means of identification

Product number -
Other names 2-benzenesulfonyl-1-methoxy-1-phenyl-ethane

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:69333-48-8 SDS

69333-48-8Downstream Products

69333-48-8Relevant articles and documents

Divergent Ritter-type amination: Via photoredox catalytic four-component radical-polar crossover reactions

Chen, Zhao-Xu,Guo, Sheng-Qiang,Jiang, Yu-Zhen,Luo, Yong-Chun,Wang, Ai-Lian,Xu, Guo-Qiang,Xu, Peng-Fei,Yang, Hui-Qing

supporting information, p. 9571 - 9576 (2021/12/09)

A green and practical divergent Ritter-type amination via a photoredox catalytic four-component radical-polar crossover process was developed. This versatile protocol presents a modular and powerful strategy to access functionalized β-sulfonyl imides and imines under mild conditions from readily available and stable substrates with high atom-, step- and redox economy. We manipulated carboxylic acids and benzotriazoles to precisely attack the nitrilium ion instead of the carbocation, thus preventing many complicated side reactions of the photocatalytic reactions. Furthermore, the synthetic utility of this divergent Ritter reaction is further demonstrated by the late-stage modification of pharmaceutical and natural product derivatives. This journal is

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