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1224599-69-2

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1224599-69-2 Usage

Type of Compound

Substituted azetidinone

Ring Structure

Four-membered heterocyclic compound

Usage

Intermediate in the synthesis of pharmaceutical compounds and agrochemicals

Key Functional Group

Strong electron-withdrawing trifluoromethyl group

Impact

Influences reactivity and properties in various chemical reactions

Importance

Building block in the production of diverse organic compounds, making it significant in the field of organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1224599-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,5,9 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1224599-69:
(9*1)+(8*2)+(7*2)+(6*4)+(5*5)+(4*9)+(3*9)+(2*6)+(1*9)=172
172 % 10 = 2
So 1224599-69-2 is a valid CAS Registry Number.

1224599-69-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4-(trifluoromethyl)azetidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:1224599-69-2 SDS

1224599-69-2Upstream product

1224599-69-2Downstream Products

1224599-69-2Relevant articles and documents

Reductive amination/cyclization of ω-trifluoromethyl keto esters to trifluoromethylated δ-amino alcohols and lactams

Wan, Wen,Hou, Jie,Jiang, Haizhen,Yuan, Zongqian,Goubin, Ma.,Zhao, Gang,Hao, Jian

experimental part, p. 1778 - 1786 (2010/06/15)

A reductive amination/cyclization approach towards biologically interesting trifluoromethylated four- to seven-membered ring lactams from simply prepared ω-trifluoromethyl keto esters in good to excellent yields has been developed. In addition, trifluorom

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