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142467-27-4

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142467-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142467-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,6 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142467-27:
(8*1)+(7*4)+(6*2)+(5*4)+(4*6)+(3*7)+(2*2)+(1*7)=124
124 % 10 = 4
So 142467-27-4 is a valid CAS Registry Number.

142467-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylcyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 3-ethylcyclohex-2-enol

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:142467-27-4 SDS

142467-27-4Relevant articles and documents

SUBSTITUTED FLUOROETHYL UREAS AS ALPHA 2 ADRENERGIC AGENTS

-

Page/Page column 44, (2008/12/04)

Therapeutic compounds, and methods, compositions, and medicaments related thereto are disclosed herein.

Exploiting the palladium[0]-catalysed Ullmann cross-coupling reaction in natural products chemistry: Application to a total synthesis of the alkaloid (±)-aspidospermidine

Banwell, Martin G.,Lupton, David W.

, p. 213 - 215 (2007/10/03)

The application of Ullmann cross-coupling reaction for the synthesis of the alkaloid (±)-aspidospermidine was studied. The initial step associated with the second stage of the synthesis of aspidospermidine involved the Pd[0]-catalyzed Ullmann cross-coupli

(2-hydroxy)ethyl-thioureas useful as modulators of alpha2B adrenergic receptors

-

, (2008/06/13)

Compounds of formula (i) and of formula (ii) wherein the symbols have the meaning disclosed in the specification, specifically or selectively modulate α2B and/or α2C adrenergic receptors in preference over α2A adrenergic receptors, and as such are useful for alleviating chronic pain and allodynia and have no or only minimal cardivascular and/or sedatory activity.

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