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2H-Pyrrol-2-one, 1,5-dihydro-1-methyl-4-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

465531-76-4

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465531-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 465531-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,5,5,3 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 465531-76:
(8*4)+(7*6)+(6*5)+(5*5)+(4*3)+(3*1)+(2*7)+(1*6)=164
164 % 10 = 4
So 465531-76-4 is a valid CAS Registry Number.

465531-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-phenylmethoxy-2H-pyrrol-5-one

1.2 Other means of identification

Product number -
Other names 4-benzyloxy-1-methylpyrrolin-2-one

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:465531-76-4 SDS

465531-76-4Relevant academic research and scientific papers

Synthesis and reactions of polymer-bound Ph3P=C=C=O: A quick route to tenuazonic acid and other optically pure 5-substituted tetramates

Schobert, Rainer,Jagusch, Carsten,Melanophy, Claire,Mullen, Gillian

, p. 3524 - 3529 (2007/10/03)

Polystyrene-bound cumulated ylide Ph3PCCO was prepared on a large scale in two steps. It reacts with Grignard compounds, amines and alcohols to give immobilized acyl, amide and ester ylides, respectively. Their Wittig reactions lead to alkenes

A new, general entry to 3,5-unsubstituted 4-O-alkyl tetramates

Paintner, Franz F.,Metz, Marcel,Bauschke, Gerd

, p. 869 - 874 (2007/10/03)

A variety of 3,5-unsubstituted 4-O-benzyl tetramates 10 was prepared in good overall yield from methyl (E)-3-benzyloxy-4-oxobut-2-enoate 7 by a reductive amination-lactamization sequence. An efficient approach to this building block as well as to various 3-alkoxy analogues is presented.

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