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2-Thiazolidinimine, 3-(phenylmethyl)-, also known as 3-benzyl-2-thiazolidinimine, is an organic compound with the chemical formula C10H10N2S. It is a derivative of thiazolidinimine, featuring a phenylmethyl group attached to the 3-position of the thiazolidinimine ring. 2-Thiazolidinimine, 3-(phenylmethyl)- is characterized by its heterocyclic structure, which includes a sulfur atom and a nitrogen atom in the ring. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity. The compound is also of interest in organic chemistry for its reactivity and potential applications in the development of new materials and compounds.

6558-46-9

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6558-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6558-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,5 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6558-46:
(6*6)+(5*5)+(4*5)+(3*8)+(2*4)+(1*6)=119
119 % 10 = 9
So 6558-46-9 is a valid CAS Registry Number.

6558-46-9SDS

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 3-benzyl-1,3-thiazolidin-2-imine

1.2 Other means of identification

Product number -
Other names 2-Imino-3-benzyl-thiazolidin

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 -
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More Details:6558-46-9 SDS

6558-46-9Relevant academic research and scientific papers

REGIOSELECTIVE HYDRIDE REDUCTION OF 2-(N-CYANOIMINO)THIAZOLIDINE DERIVATIVES

Iwata, Chuzo,Fujimoto, Michitaro,Watanabe, Mayumi,Kawakami, Tetsuya,Maeda, Noriko,et al.

, p. 2471 - 2478 (2007/10/02)

Treatment of 3-alkyl-2-(N-cyanoimino)thiazolidines with lithium aluminium hydride caused reductive cleavage of the imino double bond to afford 3-alkylthiazolidines, while diisobutylaluminum hydride reduction of 3-alkyl- and 3-sulfonyl derivatives resulted

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