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(2E)-2-(phenylmethylidene)heptanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58260-82-5

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58260-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58260-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58260-82:
(7*5)+(6*8)+(5*2)+(4*6)+(3*0)+(2*8)+(1*2)=135
135 % 10 = 5
So 58260-82-5 is a valid CAS Registry Number.

58260-82-5SDS

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 (2E)-2-benzylideneheptanenitrile

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:58260-82-5 SDS

58260-82-5Relevant academic research and scientific papers

Preparation method of nitrile compound

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Paragraph 0069-0071, (2022/01/08)

The present invention belongs to the field of organic synthesis technology, specifically relates to a method for preparing a nitrile compound, aldehyde oxime derivatives as raw materials, adding DPPA and DBU, reacting in an organic solvent, one step to pr

Organic reactions in water: An efficient zinc-mediated stereoselective synthesis of (E)- and (Z)-trisubstituted alkenes using unactivated alkyl halides

Das, Biswanath,Banerjee, Joydeep,Mahender, Gurram,Majhi, Anjoy

, p. 3349 - 3352 (2007/10/03)

(Chemical Equation Presented) Treatment of the acetyl derivatives of the Baylis-Hillman adducts 3-hydroxy-2-methylene-alkanoates and 3-hydroxy-2- methylene-alkanenitriles with unactivated alkyl halides in the presence of Zn in saturated aqueous NH4/

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