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Cyclopropanecarboxaldehyde, 1-(phenylthio)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62240-36-2

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62240-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62240-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62240-36:
(7*6)+(6*2)+(5*2)+(4*4)+(3*0)+(2*3)+(1*6)=92
92 % 10 = 2
So 62240-36-2 is a valid CAS Registry Number.

62240-36-2SDS

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 1-phenylsulfanylcyclopropane-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names Cyclopropanecarboxaldehyde,1-(phenylthio)

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:62240-36-2 SDS

62240-36-2Relevant academic research and scientific papers

Synthesizing Molecules with Linear Tricyclic 5/5/5 and 6/5/5 Skeletons via [5 + 2 + 1]/Ene Strategy

Liu, Jing,Zhou, Yi,Zhu, Jiaqi,Yu, Zhi-Xiang

supporting information, p. 7566 - 7570 (2021/10/02)

Report here is the development of a [5 + 2 + 1]/ene strategy for the synthesis of molecules with linear tricyclic 5/5/5 and 6/5/5 skeletons widely found in natural products. The first step of this strategy is applying a Rh-catalyzed [5 + 2 + 1] reaction o

Acid-catalyzed synthesis of functionalized arylthio cyclopropane carbaldehydes and ketones

Porcu, Stefania,Luridiana, Alberto,Martis, Alberto,Frongia, Angelo,Sarais, Giorgia,Aitken, David J.,Boddaert, Thomas,Guillot, Regis,Secci, Francesco

supporting information, p. 13547 - 13550 (2019/01/06)

A general strategy for the synthesis of arylthio cyclopropyl carbaldehydes and ketones via a Br?nsted acid catalyzed arylthiol addition/ring contraction reaction sequence has been exploited. The procedure led to a wide panel of cyclopropyl carbaldehydes in generally high yields and with broad substrate scope. Mechanistic aspects and synthetic applications of this procedure were investigated.

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