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Pyridinium, 4-chloro-1-(2-oxo-2-phenylethyl)-, bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63374-36-7

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63374-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63374-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,7 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63374-36:
(7*6)+(6*3)+(5*3)+(4*7)+(3*4)+(2*3)+(1*6)=127
127 % 10 = 7
So 63374-36-7 is a valid CAS Registry Number.

63374-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chloropyridin-1-ium-1-yl)-1-phenylethanone,bromide

1.2 Other means of identification

Product number -
Other names Pyridinium,4-chloro-1-(2-oxo-2-phenylethyl)-,bromide

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:63374-36-7 SDS

63374-36-7Downstream Products

63374-36-7Relevant academic research and scientific papers

Copper acetate monohydrate: A cheap but efficient oxidant for synthesizing multi-substituted indolizines from pyridinium ylides and electron deficient alkenes

Hu, Huayou,Feng, Junjun,Zhu, Yulan,Gu, Ning,Kan, Yuhe

, p. 8637 - 8644 (2012)

We report a highly practical one-pot method for synthesizing multi-substituted indolizines from ?±-halide carbonyl compounds, pyridines and electron deficient alkenes in the presence of copper acetate monohydrate and sodium acetate in DMF. A variety of function groups are tolerable in standard reaction conditions, including aldehyde. 36 examples were presented. The yield of indolizine was from moderate to high. Furthermore, multi-substituted indolizines can be prepared at gram scale by this method.

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