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105357-89-9

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105357-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105357-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,5 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105357-89:
(8*1)+(7*0)+(6*5)+(5*3)+(4*5)+(3*7)+(2*8)+(1*9)=119
119 % 10 = 9
So 105357-89-9 is a valid CAS Registry Number.

105357-89-9SDS

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-(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)ethan-1-one

1.2 Other means of identification

Product number -
Other names 1-(2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)-ethanone

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:105357-89-9 SDS

105357-89-9Relevant articles and documents

Efficient synthesis of substituted pyrroles through iron-mediated oxidation reaction of 3-methylenehexane-2,5-dione with primary amines

Chen, Xi,Yuan, JiaCheng,Zhou, Min

, p. 32 - 38 (2018/12/11)

An efficient route has been developed for the synthesis of multiple substituted pyrrole derivatives from the readily available agents through iron-mediated oxidative aromatization process in good to excellent yields. This method is well tolerated with a diverse broad range of substrates and a complementary approach to currently available synthetic methods.

Silver-catalysed hydroamination: Synthesis of functionalised pyrroles

Robinson, Ross S.,Dovey, Martin C.,Gravestock, David

, p. 6787 - 6789 (2007/10/03)

It has been shown that functionalised pyrroles can be efficiently prepared using a two-step sequence. This sequence involves the propargylation of secondary enaminones using n-BuLi and propargyl bromide, followed by intramolecular hydroamination catalysed by silver nitrate. The hydroamination can be carried out at room temperature (overnight) or in a domestic microwave oven (60 s).

Gold-Catalyzed Sequential Amination/Annulation Reactions of 2-Propynyl-1,3-dicarbonyl Compounds

Arcadi, Antonio,Di Giuseppe, Sabrina,Marinelli, Fabio,Rossi, Elisabetta

, p. 443 - 446 (2007/10/03)

The gold(III)-catalyzed sequential amination/annulation reaction of 2-propynyl-1,3-dicarbonyl compounds 1 with primary amines 2 produces 1,2,3,5-substituted pyrroles 4 in moderate to high yields.

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