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4-[1,1-dimethyl-3-(pyridin-2-yl)-2-propynyloxy]benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120281-99-4

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120281-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120281-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,8 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120281-99:
(8*1)+(7*2)+(6*0)+(5*2)+(4*8)+(3*1)+(2*9)+(1*9)=94
94 % 10 = 4
So 120281-99-4 is a valid CAS Registry Number.

120281-99-4SDS

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 4-[1,1-dimethyl-3-(pyridin-2-yl)-2-propynyloxy]benzonitrile

1.2 Other means of identification

Product number -
Other names -

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:120281-99-4 SDS

120281-99-4Relevant academic research and scientific papers

SYNTHESIS OF THE POTENT POTASSIUM CHANNEL OPENER Ro 31-6930 VIA CLAISEN REARRANGEMENT AND TANDEM REGIOCONTROLLED CYCLISATION.

Attwood, Michael R.,Churcher, Ian,Dunsdon, Rachel M.,Hurst, David N.,Jones, Philip S.

, p. 811 - 814 (1991)

The synthesis of the potent potassium channel opener Ro 31-6930 is reported.Methods of controlling the regiochemistry of the crucial cyclisation are described.

Benzopyran derivatives

-

, (2008/06/13)

Compounds of the formula STR1 wherein R 1 is hydrogen, halogen, trifluoromethyl, nitro, cyano, lower alkyl, lower alkoxycarbonyl, lower alkylthio, lower alkylsulphonyl, lower alkanoyl, aroyl, carbamoyl, mono(lower alkyl)carbamoyl or di(lower alkyl)carbamoyl, R 2 is hydrogen, lower alkyl or phenyl, R 3 is hydrogen or lower alkyl, R 4 and R 5 each is hydrogen or R 4 is hydroxy and R 5 is hydrogen or R 4 and R 5 together are a carbon-carbon bond and R 6 is an aryl or N-heteroaryl group carrying a hydroxy group in the 2-position or, in the case of a N-heteroaryl group, also a N-oxide group in the 2-position, and pharmaceutically acceptable acid addition salts of these compounds of formula I which are basic, possess pronounced potassium channel activating activity and can be used as medicaments, particularly in the control or prevention of hypertension, congestive heart failure, angina pectoris, peripheral and cerebral vascular disease and smooth muscle disorders.

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