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Ethanone, 2-(2,2-dimethyl-5-pentyl-4-thiazolidinyl)-1-phenyl-, trans- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88423-60-3

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88423-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88423-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,2 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88423-60:
(7*8)+(6*8)+(5*4)+(4*2)+(3*3)+(2*6)+(1*0)=153
153 % 10 = 3
So 88423-60-3 is a valid CAS Registry Number.

88423-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-((4S,5S)-2,2-dimethyl-5-pentylthiazolidin-4-yl)-1-phenylethan-1-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:88423-60-3 SDS

88423-60-3Downstream Products

88423-60-3Relevant academic research and scientific papers

1. BORON TRIFLURIDE ACTIVATED 3-THIAZOLINES. AN EFFICIENT PREPARATION OF FUNCTIONALIZED THIAZOLIDINES.

Meltz, Clifford N.,Volkmann, Robert A.

, p. 4503 - 4506 (2007/10/02)

Boron trifluoride activated 2,2,5-trialkyl-3-thiazolines react with a wide range of organometallic reagents to generate substituted thiazolidines.

2. BORON TRIFLURIDE ACTIVATED 3-THIAZOLINES. A VERSATILE SYNTHESIS OF THIOPHENES

Meltz, Clifford N.,Volkmann, Robert A.

, p. 4507 - 4510 (2007/10/02)

Thiazolidines generated by the addition of ketone enolates to boron trifluoride activated 2,2,5-trialkyl-3-thiazolines undergo a facile acid catalyzed conversion to di- and trisubstituted thiophenes.

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