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10270-11-8

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10270-11-8 Usage

Chemical class

Pyrrole-2,5-dione derivatives

Physical state

Yellow solid

Usage

Catalyst in chemical reactions (specifically esterification and amidation)

Application

Synthesis of pharmaceuticals and agrochemicals

Chemical property

Acts as a nucleophile

Bonding

Forms strong covalent bonds with other molecules

Importance

Valuable tool in organic synthesis

Safety precautions

Harmful if ingested or inhaled, causes skin and eye irritation, should be handled with caution

Check Digit Verification of cas no

The CAS Registry Mumber 10270-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10270-11:
(7*1)+(6*0)+(5*2)+(4*7)+(3*0)+(2*1)+(1*1)=48
48 % 10 = 8
So 10270-11-8 is a valid CAS Registry Number.

10270-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(dimethylamino)pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names N-Dimethylamino-maleinimid

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:10270-11-8 SDS

10270-11-8Downstream Products

10270-11-8Relevant articles and documents

-

Rubinstein et al.

, p. 3372 (1971)

-

Access to indoles via Diels-Alder reactions of 2-vinylpyrroles with maleimides

Noland, Wayland E.,Lanzatella, Nicholas P.,Venkatraman, Lakshmanan,Anderson, Nicholas F.,Gullickson, Glen C.

experimental part, p. 1154 - 1176 (2010/03/04)

(Chemical Equation Presented) Variously substituted 2-vinylpyrroles underwent an endo-addition [4+2] cycloaddition reaction with maleimides followed by a spontaneous highly diastereoselective (93-98% de) isomerization to give tetrahydroindoles in moderate to excellent yield. Treatment with activated MnO2 in refluxing toluene provided the corresponding indoles in moderate to good yield. This highly convergent methodology for formation of indoles is versatile and the starting materials are conveniently prepared.

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