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Butanoic acid, 4-oxo-4-[(1-phenylethyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60756-87-8

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60756-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60756-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,5 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60756-87:
(7*6)+(6*0)+(5*7)+(4*5)+(3*6)+(2*8)+(1*7)=138
138 % 10 = 8
So 60756-87-8 is a valid CAS Registry Number.

60756-87-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1-phenylethyl)-succinamic acid

1.2 Other means of identification

Product number -
Other names N-(1-phenylethyl)succinamic acid

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:60756-87-8 SDS

60756-87-8Relevant academic research and scientific papers

Regioselective synthesis of 1-alkyl-5-(indol-3-yl- and -2-yl)pyrrolidin-2- ones from available reagents

Sadovoy,Kovrov,Golubeva,Sviridova

experimental part, p. 1215 - 1223 (2011/10/09)

The reaction under mild conditions of 1-alkyl-5-hydroxypyrrolidin-2-ones with different indoles having a free 3 position leads exclusively to 1-alkyl-5-(indol-3-yl)pyrrolidin-2-ones but if position 3 is occupied to 1-alkyl-5-(indol-2-yl)pyrrolidin-2-ones.

Chemical process

-

, (2008/06/13)

A process for the preparation of a compound of the formulae (Ia) and/or (Ib): STR1 wherein R1 and R2 are independently substituted or unsubstituted hydrocarbon groups or are joined together so as to form a carbocyclic or heterocyclic ring, and R3 is a substituted or unsubstituted hydrocarbon group; which process comprises the ring-closing cyclization of a compound of the formula (II): STR2 wherein R1, R2 and R3 are as defined in relation to formulae (Ia) and (Ib).

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