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Benzene,1,1'-(1-isocyano-1,2-ethanediyl)bis-, also known as 1,1'-(1-isocyano-1,2-ethanediyl)bisbenzene or 1,2-bis(phenyl isocyanide)ethane, is an organic compound with the chemical formula C16H14N2. It is a colorless, crystalline solid that is soluble in organic solvents. Benzene,1,1'-(1-isocyano-1,2-ethanediyl)bis- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the production of polymers and resins. Due to its reactivity, it is essential to handle Benzene,1,1'-(1-isocyano-1,2-ethanediyl)bis- with care, following proper safety protocols to minimize potential health and environmental risks.

3128-88-9

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3128-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3128-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3128-88:
(6*3)+(5*1)+(4*2)+(3*8)+(2*8)+(1*8)=79
79 % 10 = 9
So 3128-88-9 is a valid CAS Registry Number.

3128-88-9SDS

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 1,2-Diphenylethylisocyanid

1.2 Other means of identification

Product number -
Other names -

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:3128-88-9 SDS

3128-88-9Downstream Products

3128-88-9Relevant academic research and scientific papers

Electrochemical synthesis of isocyanides and 1,n-diisocyanides

Hess, Ulrich,Brosig,Komenda,Schaefer

, p. 412 - 417 (2007/10/03)

Some isocyanide structures have shown fungicide, antibiotic, insecticide, akarizide and other biological activities. Electrochemical reduction of substituted tosylmethylisocyanides (TosMICs) in acetonitrile/0,1 M tetraalkylammonium supporting-electrolyte at Hg-electrodes led to new alkyl-, aryl and 1,n-diisocyanides in good yields. The reaction proceeds in a two-electron C,S-cleavage, reducing exclusively the tosyl-function. The high selectivity of the corresponding ECE-mechanism is supported by quantum- chemical calculation.

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