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1070-92-4

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1070-92-4 Usage

Description

[(ethylsulfonyl)methyl]sulfonylethane, with the molecular formula C6H14O4S2 and CAS number 38493-46-8, is a colorless liquid characterized by a strong, sweet odor. It belongs to the class of sulfonyl compounds and is recognized for its utility as an intermediate in the synthesis of a wide range of organic compounds. This chemical's reactivity and capacity to form more complex molecules make it a valuable asset in the pharmaceutical and agricultural sectors.

Uses

Used in Pharmaceutical Industry:
[(ethylsulfonyl)methyl]sulfonylethane is used as a synthetic intermediate for the development of various drugs. Its unique structure allows it to be a building block for more complex pharmaceutical compounds, contributing to the creation of novel medications with potential therapeutic benefits.
Used in Agricultural Industry:
In the agricultural sector, [(ethylsulfonyl)methyl]sulfonylethane serves as a key intermediate in the synthesis of pesticides. Its incorporation into the chemical structure of these products can enhance their effectiveness in controlling pests and protecting crops.
Used in Chemical Synthesis:
[(ethylsulfonyl)methyl]sulfonylethane is also utilized as a versatile intermediate in the synthesis of other chemical products. Its reactive properties enable it to be a component in the formation of a diverse array of compounds, expanding its applications across various industries.
Safety Precaution:
While [(ethylsulfonyl)methyl]sulfonylethane offers numerous applications in chemical synthesis, it is essential to handle it with care due to its potential to cause skin and eye irritation. Proper safety measures should be taken to minimize any adverse effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 1070-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1070-92:
(6*1)+(5*0)+(4*7)+(3*0)+(2*9)+(1*2)=54
54 % 10 = 4
So 1070-92-4 is a valid CAS Registry Number.

1070-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(ethylsulfonylmethylsulfonyl)ethane

1.2 Other means of identification

Product number -
Other names bis(ethylsulfonyl)methane

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:1070-92-4 SDS

1070-92-4Relevant articles and documents

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Hough,Taylor

, p. 1212,1216 (1955)

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POLYSULFONYLETHYLENES. COMMUNICATION 2. THE REACTION OF TETRAKISALKYLSULFONYLETHENES WITH WATER, ALCOHOLS, AND THIOLS

Petukhova, N. P.,Dontsova, N. E.,Prilezhaeva, E. N.

, p. 173 - 178 (2007/10/02)

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Pterins. VIII. The Absolute Configuration at C 6 of Natural 2-Amino-6--5,6,7,8-tetrahydropteridin-4(3H)-one (L-erythro-5,6,7,8-tetrahydrobiopterin)

Armarego, Wilfred L. F.,Waring, Paul,Paal, Bela

, p. 785 - 793 (2007/10/02)

The conformation of the side chain of 5,6,7,8-tetrahydrobiopterin (6) in 0.5 M DCl/D2O is predominantly quasi-equatorial (deduced from 3J (13C 4a, 1H 6) 1.1 Hz), and is the same as that of the methyl group in 2-methyl-1,2,3,4-tetrahydroquinoxaline and in 2-amino-6-methyl-5,6,7,8-tetrahydropteridin-4(3H)-one in the same solvent.Because (-)-2S)-2-methyl-1,2,3,4-tetrahydroquinoxaline (4) and (-)-(6S)-2-amino-6-methyl-5,6,7,8-tetrahydropteridin-4(3H)-one (5) have the same conformation and negative c.d. spectra (Θ 248 nm and 263 nm respectively) as does the natural 5,6,7,8-tetrahydrobiopterin (Θ minimum at 265 nm) in 0.1 M hydrochloric acid, then the absolute conformations of the tetrahydropyrazine rings and the absolute configurations at the chiral crntres C2, C6, and C6 of compounds (4),(5) and (6) respectively are the same.Hence the absolute configuration at C6 in natural 5,6,7,8-tetrahydrobiopterin is R.A convenient synthesis of biopterrin on a gram scale is described.

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