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Methanesulfonic acid, trifluoro-, 4-(dipropylamino)-1-cyclohexen-1-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

262427-72-5

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262427-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 262427-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,4,2 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 262427-72:
(8*2)+(7*6)+(6*2)+(5*4)+(4*2)+(3*7)+(2*7)+(1*2)=135
135 % 10 = 5
So 262427-72-5 is a valid CAS Registry Number.

262427-72-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trifluoromethanesulfonic acid 4-dipropylaminocyclohex-1-enyl ester

1.2 Other means of identification

Product number -
Other names Trifluoro-methanesulfonic acid 4-dipropylamino-cyclohex-1-enyl 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:262427-72-5 SDS

262427-72-5Relevant academic research and scientific papers

Conjugated enynes as nonaromatic catechol bioisosteres: Synthesis, binding experiments, and computational studies of novel dopamine receptor agonists recognizing preferentially the D3 subtype

Hübner, Harald,Haubmann, Christian,Utz, Wolfgang,Gmeiner, Peter

, p. 756 - 762 (2000)

To evaluate nonaromatic catechol bioisosteres, the conformationally restrained enynes I and enediynes 2 were synthesized via palladium-catalyzed coupling as the key reaction step. Subsequent receptor binding studies at the dopamine receptor subtypes Dsub

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