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88718-80-3

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88718-80-3 Usage

Class

Naphthalene compounds

Structure

Naphthalene core with an imidazole ring fused at two adjacent carbon atoms and a vinyl group (1-ethenyl) attached to the imidazole ring

Type

Organic compound

Industrial applications

Component in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Potential uses

Development of new materials, dyes, and other chemical products

Unique properties

Molecular structure and properties of 1H-Naphth[2,3-d]imidazole,1-ethenyl-(9CI) make it useful in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 88718-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,1 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88718-80:
(7*8)+(6*8)+(5*7)+(4*1)+(3*8)+(2*8)+(1*0)=183
183 % 10 = 3
So 88718-80-3 is a valid CAS Registry Number.

88718-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Vinyl-1H-naphtho[2,3-d]imidazole

1.2 Other means of identification

Product number -
Other names 1-vinyl-indanol

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:88718-80-3 SDS

88718-80-3Downstream Products

88718-80-3Relevant articles and documents

VINYLATION OF NAPHTHOIMIDAZOLE

Lopyrev, V. A.,Kuznetsova, N. P.,Myachina, G. F.,Ermakova, T. G.

, p. 1219 - 1221 (1983)

1-vinylnaphthoimidazole has been synthesized by reacting naphthoimidazole with vinyl acetate in the presence of mercuric acetate, as well as with acetylene under pressure in the presence of potassium hydroxide.

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