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Ethyl (thiophen-2-ylmethyl)carbamate is a chemical compound with the molecular formula C8H11NOS2. It is an organic compound that belongs to the class of carbamates, which are derivatives of carbamic acid. This specific compound features a thiophene ring, which is a five-membered aromatic ring with one sulfur atom, and an ethyl group attached to the carbamate functional group. Ethyl (thiophen-2-ylmethyl)carbamate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is an important intermediate in the preparation of certain biologically active molecules, and its properties can be further explored for the development of new compounds with specific therapeutic or pesticidal effects.

6268-34-4

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6268-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6268-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6268-34:
(6*6)+(5*2)+(4*6)+(3*8)+(2*3)+(1*4)=104
104 % 10 = 4
So 6268-34-4 is a valid CAS Registry Number.

6268-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2]thienylmethyl-carbamic acid ethyl ester

1.2 Other means of identification

Product number -
Other names [2]Thienylmethyl-carbamidsaeure-aethylester

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:6268-34-4 SDS

6268-34-4Downstream Products

6268-34-4Relevant academic research and scientific papers

Direct reductive amination using triethylsilane and catalytic bismuth(III) chloride

Matsumura, Takehiko,Nakada, Masahisa

, p. 1829 - 1834 (2014/03/21)

Direct reductive amination (DRA) using triethylsilane (TESH) and catalytic bismuth(III) chloride (BiCl3) is described for the first time. The use of TESH and BiCl3 provides easy handling, low cost, non-toxicity, and a mild Lewis acid activity, thereby meeting the demand for green and sustainable chemistry. The developed DRA is highly chemoselective and applicable to less-basic amines. The experimental results of this study revealed that the developed DRA could be catalyzed by BiCl3, which was gradually reduced to Bi(0) or bismuth with a low valency by TESH, but TESCl, Bi(0), and Bi(0) with TESCl catalyzed the DRA to some extent.

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