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1-Azabicyclo[2.2.2]octan-3-ol, benzenesulfonate (ester) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64099-43-0

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64099-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64099-43-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64099-43:
(7*6)+(6*4)+(5*0)+(4*9)+(3*9)+(2*4)+(1*3)=140
140 % 10 = 0
So 64099-43-0 is a valid CAS Registry Number.

64099-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylsulphonyloxy-quinuclidine

1.2 Other means of identification

Product number -
Other names Benzenesulfonic acid 1-aza-bicyclo[2.2.2]oct-3-yl ester

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:64099-43-0 SDS

64099-43-0Downstream Products

64099-43-0Relevant academic research and scientific papers

Identification of Bond-Weakening Spirosilane Catalyst for Photoredox α-C?H Alkylation of Alcohols

Sakai, Kentaro,Oisaki, Kounosuke,Kanai, Motomu

, p. 337 - 343 (2020)

The development of catalyst-controlled site-selective C(sp3)?H functionalization is a current major challenge in organic synthesis. This paper describes DFT-guided identification of pentavalent silicate species as a novel bond-weakening catalyst for the α-C?H bonds of alcohols together with a photoredox catalyst and a hydrogen atom transfer catalyst. Specifically, Martin's spirosilane accelerated α-C?H alkylation of alcohols. (Figure presented.).

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