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927829-33-2

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927829-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 927829-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,7,8,2 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 927829-33:
(8*9)+(7*2)+(6*7)+(5*8)+(4*2)+(3*9)+(2*3)+(1*3)=212
212 % 10 = 2
So 927829-33-2 is a valid CAS Registry Number.

927829-33-2SDS

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-(4-cyanophenyl)-3-dimethylamino-2-propen-1-one

1.2 Other means of identification

Product number -
Other names 1-(4-cyanophenyl)-3-dimethylaminopropen-1-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:927829-33-2 SDS

927829-33-2Relevant articles and documents

Synthesis and complexes of the new scorpionate ligand tris[3-(4- benzonitrile)-pyrazol-1-yl]borate

Batten, Stuart R.,Duriska, Martin B.,Jensen, Paul,Lu, Jinzhen

, p. 72 - 74 (2007)

A new scorpionate ligand, hydro-tris[3-(4-benzonitrile)-pyrazol-1-yl]borate (Tp4bz), was synthesized and the crystal structures of its potassium salt and its MnII, CoII, NiII, and Cd II complexes were

Highly Site-Selective Metal-Free C-H Acyloxylation of Stable Enamines

Wang, Fei,Sun, Wangbing,Wang, Yixin,Jiang, Yaojia,Loh, Teck-Peng

supporting information, p. 1256 - 1260 (2018/02/23)

A highly site-selective acyloxylation of stable enamines with PhI(OAc)2 under metal-free conditions to afford (E)-vinyl acetate derivatives in good to excellent yields is described. Depending on the judicious choice of the solvent system, either the α- or β-site-selective product could be obtained with high selectivity. For the α-site-selective product, the rearranged amide compound is obtained as the major product. This reaction proceeds under mild reaction conditions (room temperature, metal-free, and open-flask) and features a broad substrate scope.

Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization

Liang, Gaohui,Rong, Jiaxin,Sun, Wangbin,Chen, Gengjia,Jiang, Yaojia,Loh, Teck-Peng

supporting information, (2018/11/23)

An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a

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