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162934-76-1

162934-76-1

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162934-76-1 Usage

Chemical Properties

Brown Foam

Uses

Nnaphthalen-1-yl(1H-pyrrol-3-yl)methanone is used in the preparation of high affinity ligands for the cannabinoid CB1 and CB2 receptors.

Check Digit Verification of cas no

The CAS Registry Mumber 162934-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,9,3 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 162934-76:
(8*1)+(7*6)+(6*2)+(5*9)+(4*3)+(3*4)+(2*7)+(1*6)=151
151 % 10 = 1
So 162934-76-1 is a valid CAS Registry Number.

162934-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Naphthalen-1-yl(1H-pyrrol-3-yl)methanone

1.2 Other means of identification

Product number -
Other names naphthalen-1-yl(1H-pyrrol-3-yl)methanone

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:162934-76-1 SDS

162934-76-1Relevant articles and documents

Imidazole derivatives having an inhibitory activity for farnesyl transferase and process for preparation thereof

-

, (2008/06/13)

The present invention relates to a novel imidazole derivative represented by formula (1) which shows an inhibitory activity against farnesyl transferase or pharmaceutically acceptable salts or isomers thereof, in which A, n1and Y are defined in the specification; to a process for preparation of the compound of formula (1); to intermediates which are used in the preparation of the compound of formula (1); and to a pharmaceutical composition comprising the compound of formula (1) as an active ingredient.

The regioselective photoinduced aroylation at the 3-position of pyrrole derivatives

Oda, Kazuaki,Hiratsuka, Rin,Machida, Minoru

, p. 463 - 470 (2007/10/03)

Irradiation of arenecarbothioamide with pyrrole or indole derivatives gave regioselectively 3-aroylpyrrole or -indole derivatives, respectively.

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