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19036-56-7

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19036-56-7 Usage

Structure

Cycloheptane ring with a hydroxyl group at the 1-position and a carbonitrile group attached
The compound is composed of a seven-carbon ring structure with a hydroxyl (-OH) group attached to the first carbon and a cyano (-CN) group attached to the ring.

Usage

Building block in organic synthesis and pharmaceutical research
1-hydroxycycloheptanecarbonitrile is utilized as an intermediate compound in the production of various other chemical compounds, particularly in the fields of organic synthesis and pharmaceutical research.

Potential applications

Development of pharmaceuticals and agrochemicals
Due to its unique chemical properties, 1-hydroxycycloheptanecarbonitrile has potential applications in the creation of new pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 19036-56-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,3 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19036-56:
(7*1)+(6*9)+(5*0)+(4*3)+(3*6)+(2*5)+(1*6)=107
107 % 10 = 7
So 19036-56-7 is a valid CAS Registry Number.

19036-56-7SDS

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-hydroxycycloheptane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-hydroxy-cycloheptanecarbonitrile

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:19036-56-7 SDS

19036-56-7Relevant articles and documents

Synthesis, spectral, and structural characteristics of cyanohydrines derived from aliphatic cyclic ketones1

Hosten,Betz

, p. 2222 - 2227 (2014)

A series of cyanohydrines derived from cyclic aliphatic ketones was synthesized by acid-catalyzed nucleophilic addition reaction under the action of potassium cyanide. The products were characterized by means of multi-nuclear NMR spectroscopy (1H, 13C, 14N, 15N), mass spectrometry, elemental analysis, UV-Vis spectroscopy, refraction index measurements as well as vibrational spectroscopy. The structure of the cyanohydrine of cyclohexanone was elucidated by means of single crystal X-ray diffraction.

Synthesis of Succinonitrile Derivatives by Homocoupling from Cyanohydrin Derivatives with a Low-Valent Titanium Reagent

Matsunaga, Kazuma,Endo, Ryusei,Nagasawa, Kokoro,Kishida, Atsushi,Takatori, Kazuhiko

supporting information, p. 3707 - 3711 (2022/02/07)

A method is described for synthesizing succinonitrile derivatives bearing alkyl or aryl substituents from cyanohydrin derivatives using low-valent titanium. The active species in this reaction is proposed to be a resonance hybrid of the TiIV nitrile enolate and TiIII alkyl radical.

Studies on phosphoroheterocycle chemistry III: An unusual way to 1,3,2-thiazaphospholidine-4-thione 2-sulfide derivatives

Deng, ShengLou,Chen, RuYu

, p. 2527 - 2531 (2007/10/03)

An unusual but efficient method for the synthesis of phosphoroheterocycles, 1,3,2-thiazaphospholidine-4-thione 2-sulfide derivatives, by the reaction of Lawesson's reagent with a variety of α-hydroxy nitriles has been developed. The possible mechanism of the reaction is proposed to involve thiation of hydroxy group in a first step, sequential addition of P-SH to the nitrile and rearrangement resulting in the title phosphoroheterocycles. The preliminary bioassays show that these heterocyclic compounds have herbicidal properties.

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