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15619-19-9

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15619-19-9 Usage

General Description

4α-tert-Butylcyclohexane-1α-carbonitrile is a chemical compound with the molecular formula C13H21N. It is a cyanide derivative of tert-butylcyclohexane and is commonly used in organic synthesis and pharmaceutical research. The compound has a cyclic structure with a tert-butyl group attached to the 4th carbon atom and a nitrile group attached to the 1st carbon atom. It is a colorless liquid with a characteristic odor and is soluble in organic solvents. 4α-tert-Butylcyclohexane-1α-carbonitrile is often used as a precursor in the production of various pharmaceuticals and agrochemicals. It is important to handle this compound with caution and follow proper safety protocols when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 15619-19-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,1 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15619-19:
(7*1)+(6*5)+(5*6)+(4*1)+(3*9)+(2*1)+(1*9)=109
109 % 10 = 9
So 15619-19-9 is a valid CAS Registry Number.

15619-19-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-4-tert-Butylcyclohexanecarbonitrile

1.2 Other means of identification

Product number -
Other names cis-4-t-butylcyclohexanecarbonitrile

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:15619-19-9 SDS

15619-19-9Downstream Products

15619-19-9Relevant articles and documents

DIASTEREOSELECTIVE PROTONIERUNG VON CARBANIONEN

Gerlach, Uve,Huenig, Siegfried

, p. 5805 - 5808 (1987)

Despite of very small side differentiation in 3-Li the ratio of cis-3: trans-3 can be shifted from 41: 59 to 85: 15 by variation of the proton sources.

Oxoammonium salt-mediated oxidative nitriles synthesis from aldehydes with ammonium acetate

Kim, Myeong Jin,Mun, Junyoung,Kim, Jinho

supporting information, p. 4695 - 4698 (2017/11/17)

An efficient and scalable route for the synthesis of nitriles was developed by oxoammonium salt (4-acetamido-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate) mediated oxidative conversion of aldehydes with NH4OAc. A variety of aliphatic aldehydes as well as benzaldehydes were converted into the corresponding nitriles in high yields. The nitroxyl radical which is the reduced species of the used oxoammonium salt was recovered by simple acid-base extraction for the recycling.

Electrochemical oxidation of ketone acylhydrazones and their HCN adducts in NaCN-MeOH. Tranformation of ketones to nitriles

Okimoto,Chiba

, p. 1070 - 1076 (2007/10/02)

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