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1-Cyclohexene-1-carboxylic acid, 5-(1,1-dimethylethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62222-98-4

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62222-98-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62222-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,2 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62222-98:
(7*6)+(6*2)+(5*2)+(4*2)+(3*2)+(2*9)+(1*8)=104
104 % 10 = 4
So 62222-98-4 is a valid CAS Registry Number.

62222-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-tert-butylcyclohexene-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Cyclohexene-1-carboxylic acid,5-(1,1-dimethylethyl)-,ethyl ester

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:62222-98-4 SDS

62222-98-4Downstream Products

62222-98-4Relevant academic research and scientific papers

An expedient, stereoselective synthesis of highly functionalized cyclic compounds

Krawczyk, Ewa,Owsianik, Krzysztof,Skowronska, Aleksandra,Wieczorek, Michal,Majzner, Wieslaw

, p. 1753 - 1767 (2007/10/03)

New thiophosphates containing functionalized cyclic ketone derivatives as ligands have been stereoselectively (prepared from readily available starting materials. Full axial stereoselectivity of the NaBH)4 (reduction) of the carbonyl group in thiophosphates providing the corresponding thiols or sulfides has been demonstrated. The sulfides have been transformed into new functionalized cyclic Baylis-Hillman type adducts of defined configuration. The prospects for the useful synthetic application of these adducts appear to be very promising.

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