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3-Pentenenitrile, 2-(benzoyloxy)-, also known as 2-(benzoyloxy)-3-pentenenitrile, is an organic compound with the chemical formula C12H11NO2. It is a colorless to pale yellow liquid with a molecular weight of 203.22 g/mol. 3-Pentenenitrile, 2-(benzoyloxy)- is characterized by the presence of a pentene backbone with a nitrile group at the 3-position and a benzoyloxy group at the 2-position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and other specialty chemicals. Due to its reactivity and potential applications, it is important to handle 3-Pentenenitrile, 2-(benzoyloxy)- with care, following appropriate safety protocols.

1591-16-8

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1591-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1591-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1591-16:
(6*1)+(5*5)+(4*9)+(3*1)+(2*1)+(1*6)=78
78 % 10 = 8
So 1591-16-8 is a valid CAS Registry Number.

1591-16-8SDS

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-cyanobut-2-enyl benzoate

1.2 Other means of identification

Product number -
Other names (E)-2-(benzoyloxy)pent-3-enenitrile

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:1591-16-8 SDS

1591-16-8Relevant academic research and scientific papers

Solvent-free synthesis of cyanohydrin derivatives catalysed by triethylamine

Baeza, Alejandro,Najera, Carmen,Retamosa, Ma. De Gracia,Sansano, Jose M.

, p. 2787 - 2797 (2007/10/03)

A very simple one-step environmentally friendly procedure for the synthesis of O-substituted cyanohydrins from aldehydes and ketones, in the absence of solvent, employing minimum amounts of the corresponding cyanides has been optimised. Aldehydes react more rapidly than ketones using triethylamine as catalyst offering in both cases almost quantitative yields of the corresponding O-trimethylsilyl, O-methoxycarbonyl, O-benzoyl and O-acetyl cyanohydrins. Georg Thieme Verlag Stuttgart.

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