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1,3-Dithiolane-2-carbonyl chloride, 4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39098-96-9

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39098-96-9 Usage

Structure

A carbonyl chloride derivative of 1,3-dithiolane, which is a heterocyclic compound containing a five-membered ring with two sulfur atoms and one oxygen atom.

Functional groups

Carbonyl chloride, heterocyclic ring, and a methyl group.

Uses

Typically used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

Reactivity

Highly reactive compound.

Safety precautions

Potential for causing skin and eye irritation, as well as respiratory and digestive tract irritation. Should be handled with care and only used in a controlled laboratory setting by trained professionals.

Regulation

1,3-Dithiolane-2-carbonyl chloride, 4-methyl(9CI) is a regulated substance.

Check Digit Verification of cas no

The CAS Registry Mumber 39098-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,9 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39098-96:
(7*3)+(6*9)+(5*0)+(4*9)+(3*8)+(2*9)+(1*6)=159
159 % 10 = 9
So 39098-96-9 is a valid CAS Registry Number.

39098-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1,3-dithiolane-2-carbonyl chloride

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:39098-96-9 SDS

39098-96-9Relevant academic research and scientific papers

Synthesis of β-Lactams via Ketene-Imine Cycloaddition Chiral Ketenes Bearing a 1,3-Dithiolane Ring

Abramski, Wojciech,Belzecki, Czeslaw,Chmielewski, Marek

, p. 451 - 457 (2007/10/02)

The reaction of chlorides and ketenes derived from 1,3-dithiolane-2-carboxylic acid and Schiff's bases affords substituted β-lactams.Introduction of chirality into the dithiolane residue leads to diastereoface-differentiation in formation of the four-membered ring.

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