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2-Propen-1-amine, N-[(2-methoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42551-56-4

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42551-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42551-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,5 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42551-56:
(7*4)+(6*2)+(5*5)+(4*5)+(3*1)+(2*5)+(1*6)=104
104 % 10 = 4
So 42551-56-4 is a valid CAS Registry Number.

42551-56-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name monoselenotetrathionate(2-)

1.2 Other means of identification

Product number -
Other names Monoselenotetrathionat(2-)

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:42551-56-4 SDS

42551-56-4Relevant academic research and scientific papers

Photo-induced intramolecular arene-olefin meta-cycloaddition of 5-phenyl-fluorinated-pent-1-enes

Guo, Xiao-Chuan,Chen, Qing-Yun

, p. 149 - 156 (1999)

A series of fluorinated angular and linear triquinanes and their aza-analogues have been synthesized by photo-induced intramolecular meta-cycloaddition of 5-phenyl-fluorinated-pent-1-enes.

A versatile multi-component one-pot thiazole synthesis

Heck, Stefan,D?mling, Alexander

, p. 424 - 426 (2007/10/03)

A new multi-component reaction (MCR) of oxo components, primary amines, thiocarboxylic acids and a special isocyanide yielding 2,4-disubstituted thiazoles is described. This one-pot, one-step reaction is an alternative to current methods of thiazole ring formation and can be applied to combinatorial chemistry as well as in the total synthesis of thiazole containing natural products.

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