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Pyridine, 1,2,3,4-tetrahydro-6-(1-hydroxycyclobutyl)-1-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

353248-22-3

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353248-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 353248-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,2,4 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 353248-22:
(8*3)+(7*5)+(6*3)+(5*2)+(4*4)+(3*8)+(2*2)+(1*2)=133
133 % 10 = 3
So 353248-22-3 is a valid CAS Registry Number.

353248-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[1-(toluene-4-sulfonyl)-1,4,5,6-tetrahydropyridin-2-yl]-cyclobutanol

1.2 Other means of identification

Product number -
Other names 1-[1-(Toluene-4-sulfonyl)-1,4,5,6-tetrahydro-pyridin-2-yl]-cyclobutanol

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:353248-22-3 SDS

353248-22-3Relevant academic research and scientific papers

Synthesis of functionalized 1-azaspirocyclic cyclopentanones using bronsted acid or N-bromosuccinimide promoted ring expansions

Dake, Gregory R.,Fenster, Michael D. B.,Hurley, Paul B.,Patrick, Brian O.

, p. 5668 - 5675 (2007/10/03)

Azaspirocyclic ring systems are present in a variety of alkaloids. Functionalized 1-azaspirocyclopentanones (6, 7, 11, 12) can be efficiently constructed through semipinacol ring expansion reactions of 2-(1- hydroxycyclobutyl)-p-toluenesulfonylenamides (4

Construction of Azaspirocyclic Ketones through α-Hydroxyiminium Ion or α-Siloxy Epoxide Semipinacol Rearrangements

Fenster, Michael D. B.,Patrick, Brian O.,Dake, Gregory R.

, p. 2109 - 2112 (2007/10/03)

(matrix presented) method 1: R,R1=H, n=1 method 2: R=TMS, R1=OH, n=2 Semipinacol-type rearrangements to produce azaspirocyclic ketones are presented. The yields and stereoselectivities of these reactions range from 67-94% yield and 2

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