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Cyclohexanecarbonitrile, 4-(1,1-dimethylethyl)-1-methyl-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15619-22-4

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15619-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15619-22-4 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, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15619-22:
(7*1)+(6*5)+(5*6)+(4*1)+(3*9)+(2*2)+(1*2)=104
104 % 10 = 4
So 15619-22-4 is a valid CAS Registry Number.

15619-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-1-methylcyclohexanecarbonitrile

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-1-methyl-cyclohexanecarbonitrile

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:15619-22-4 SDS

15619-22-4Relevant academic research and scientific papers

Cyclic nitriles: Diastereoselective alkylations

Fleming, Fraser F.,Gudipati, Subrahmanyam,Zhang, Zhiyu,Liu, Wang,Steward, Omar W.

, p. 3845 - 3849 (2007/10/03)

Diastereoselective alkylations of metalated conformationally locked 4-tert-butylcyclohexanecarbonitrile are highly diastereoselective with magnesium and copper counterions but only modestly diastereoselective with lithium as the counterion. Selective gene

Metalated Nitriles: Halogen - Metal Exchange with α-Halonitriles

Fleming, Fraser F.,Zhang, Zhiyu,Knochel, Paul

, p. 501 - 503 (2007/10/03)

(Equation presented) α-Halonitriles react with organometallic reagents in a facile halogen-metal exchange. The halogen-metal exchange is extremely fast with Grignard and alkyllithium reagents, generating metalated nitriles in situ with aldehyde, ketone, a

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