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2-Benzyl-2-methyl-1,3-thiazolidine is a heterocyclic organic compound characterized by a five-membered ring containing sulfur and nitrogen atoms. It is a derivative of the 1,3-thiazolidine class of compounds, with a benzyl group attached to the 2-position and a methyl group at the same position. 2-benzyl-2-methyl-1,3-thiazolidine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as a building block in the creation of more complex molecules, particularly those with biological activity. The compound's properties, such as its stability and the ability to form various functional groups, make it a valuable intermediate in organic synthesis.

773-46-6

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773-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773-46-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 773-46:
(5*7)+(4*7)+(3*3)+(2*4)+(1*6)=86
86 % 10 = 6
So 773-46-6 is a valid CAS Registry Number.

773-46-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-2-methyl-thiazolidine

1.2 Other means of identification

Product number -
Other names (+-)-2-Benzyl-2-methyl-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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:773-46-6 SDS

773-46-6Relevant academic research and scientific papers

Phenyliodine(III) Diacetate/I2-Mediated Domino Approach for Pyrrolo[1,4]Thiazines and 1,4-Thiazines by a One-Pot Morin Rearrangement of N,S-Acetals

Danton, Fanny,Othman, Mohamed,Lawson, Ata Martin,Moncol, Ján,Ghinet, Alina,Rigo, Beno?t,Da?ch, Adam

, p. 6113 - 6118 (2019/04/17)

An efficient domino transformation using a phenyliodine(III) diacetate (PIDA)/I2 combination towards Morin 1,4-thiazine compounds has been developed starting from N,S-acetals. The latter leads to “one-step” regioselective methylene insertion without the need for traditional sulfoxide intermediates in good yields. The reaction involves easily accessible N,S-acetals obtained from cost-effective basic ketones and cysteamine as starting materials. This process ultimately leads to 1,4-thiazines related to natural product and fused derivatives necessary for further QSAR study.

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