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15395-91-2

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15395-91-2 Usage

Type of compound

Cyclic urea derivative

Physical state at room temperature

Colorless, crystalline solid

Usage

Crosslinking agent in polymer and resin production

Applications

Manufacturing of adhesives and coatings

Industrial benefits

Improves mechanical properties and thermal stability of materials

Additional uses

Synthesis of pharmaceuticals and agrochemicals

Safety precautions

Can cause skin, eye, and respiratory irritation; handle with care and follow safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 15395-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15395-91:
(7*1)+(6*5)+(5*3)+(4*9)+(3*5)+(2*9)+(1*1)=122
122 % 10 = 2
So 15395-91-2 is a valid CAS Registry Number.

15395-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(2-oxopyrrolidin-1-yl)ethyl]pyrrolidin-2-one

1.2 Other means of identification

Product number -
Other names 2-Pyrrolidinone,1,1'-(1,2-ethanediyl)bis

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:15395-91-2 SDS

15395-91-2Downstream Products

15395-91-2Relevant articles and documents

Synthesis of new N-substituted 2-pyrrolidinones via homogeneous catalytic reactions catalyzed by Pt and Rh complexes

Kollar, Laszlo,Heil, Balint,Sandor, Peter

, p. 191 - 194 (2007/10/02)

1-Vinyl-2-pyrrolidinone undergoes under oxo-conditions selective dimerization in the presence of Pt complexes and hydroformylation in the presence of Rh complexes.Theyield and regioselectivity of the Rh-catalyzed hydroformylation strongly depend on the type of phosphine present on the metal.

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