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106881-77-0

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106881-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106881-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,8 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106881-77:
(8*1)+(7*0)+(6*6)+(5*8)+(4*8)+(3*1)+(2*7)+(1*7)=140
140 % 10 = 0
So 106881-77-0 is a valid CAS Registry Number.

106881-77-0SDS

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 (1E)-N-Hydroxy-1-(3-pyridinyl)ethanimine

1.2 Other means of identification

Product number -
Other names (E)-1-propyl 3-(4-hydroxy-3-methoxyphenyl)acrylate

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:106881-77-0 SDS

106881-77-0Relevant articles and documents

Unusual course of the p-nitrophenyl phosphate esters cleavage by 3-hydroxyiminoalkylpyridinium salts in micellar solutions

Kotoucova, Hana,Mazac, Jiri,Cibulka, Radek,Hampl, Frantisek,Liska, Frantisek

, p. 649 - 650 (1998)

Two types of amphiphilic quaternary 3-pyridinium ketoximes with different position of the hydrophobic alkyl chain were synthesized and tested as hydrolytic micellar catalysts. A considerable positive deviation from the expected first-order curve was observed in the absorbance vs time plot when p-nitrophenyl diphenyl phosphate and p-nitrophenyl diethyl phosphate were hydrolyzed in micellar solutions of the prepared ketoximes under pseudo-first-order reaction conditions.

Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate

Ishihara, Kotaro,Shioiri, Takayuki,Matsugi, Masato

supporting information, p. 1295 - 1298 (2019/04/13)

A novel method for the stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via the Beckmann rearrangement was developed using diphenyl phosphorazidate (DPPA) as both the oxime activator and azide source. Various ketoximes were transformed into the corresponding 1,5-disubstituted tetrazoles with exclusive trans-group migration and no E-Z isomerization of the ketoxime. This method enables the preparation of 1,5-disubstituted tetrazoles without using toxic or explosive azidation reagents.

Modulation of PPAR subtype selectivity. Part 2: Transforming PPARα/γ dual agonist into α selective PPAR agonist through bioisosteric modification

Zaware, Pandurang,Shah, Shailesh R.,Pingali, Harikishore,Makadia, Pankaj,Thube, Baban,Pola, Suresh,Patel, Darshit,Priyadarshini, Priyanka,Suthar, Dinesh,Shah, Maanan,Jamili, Jeevankumar,Sairam, Kalapatapu V.V.M.,Giri, Suresh,Patel, Lala,Patel, Harilal,Sudani, Hareshkumar,Patel, Hiren,Jain, Mukul,Patel, Pankaj,Bahekar, Rajesh

scheme or table, p. 628 - 632 (2011/03/18)

A novel series of oxime containing benzyl-1,3-dioxane-r-2-carboxylic acid derivatives (6a-k) were designed as selective PPARα agonists, through bioisosteric modification in the lipophilic tail region of PPARα/γ dual agonist. Some of the test compounds (6a

Catalytic enantioselective borane reduction of benzyl oximes: Preparation of (S)-1-pyridin-3-YL-ethylamine bis hydrochloride

Huang, Kun,Ortiz-Marciales, Margarita,Hughes, David

experimental part, p. 36 - 52 (2011/05/13)

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