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Cyclohexaneacetonitrile, 1-fluoro-α-hydroxy, also known as 1-fluoro-2-hydroxycyclohexaneacetonitrile, is a chemical compound with the molecular formula C7H11FNO. It is a derivative of cyclohexane, featuring a nitrile group (-CN) attached to the acetone moiety, and a fluorine atom and hydroxyl group (-OH) at the 1st and 2nd carbon positions, respectively. Cyclohexaneacetonitrile, 1-fluoro--alpha--hydroxy- is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals, due to its unique structure and potential reactivity. It is a colorless to pale yellow liquid with a density of 1.1 g/cm3 and a melting point of 40-42°C. The compound is sensitive to light and heat, and it is typically stored in a cool, dry place away from direct sunlight.

699-43-4

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699-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 699-43-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 699-43:
(5*6)+(4*9)+(3*9)+(2*4)+(1*3)=104
104 % 10 = 4
So 699-43-4 is a valid CAS Registry Number.

699-43-4SDS

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 α-(1-Fluorocyclohexyl)-α-hydroxyacetonitrile

1.2 Other means of identification

Product number -
Other names 1-Fluor-1-cyanhydroxymethyl-cyclohexan

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:699-43-4 SDS

699-43-4Relevant academic research and scientific papers

NOUVELLE VOIE DE SYNTHESE D'ACIDES AMINES MONOFLUORES

Ayi, A. I.,Remli, M.,Guedj, R.

, p. 1505 - 1508 (2007/10/02)

Ring opening of the glycidonitriles (IIa-e) by HF/pyridine leads to the fluorocyanohydrins (IIIa-e).Treatment of the nitriles (IIIa-e) with ammonia in methanol gives the α-amino-β-fluoro nitriles (IVa-e) which upon acidic hydrolysis afford the β-fluoro-α-

NEW SYNTHETIC ROUTES TO β-FLUORO β-PHENYLLACTIC ACID DERIVATIVES AND Β-FLUOROCYANOHYDRINS

Ayi, A. I.,Remli, M.,Condom, R.,Guedj, R.

, p. 565 - 580 (2007/10/02)

Alkyl phenyl 2,3-epoxycarboxylates from the well-known Darzens glycidic esters synthesis react under very mild conditions with pyridinium-poly-hydrogen fluoride to give corresponding 3-fluoro 3-phenyllactates in almost quantitative yields with a high regio and stereoselectivity.This method can be applied succesfully to other flycidic derivatives: glycidoamides, glycidonitriles, glycidoiminoesters...The spectrometric properties (IR, NMR) are presented.

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