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91905-68-9

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91905-68-9 Usage

Description

[(2,2-diethoxyethyl)sulfanyl]methylbenzene is a complex organic compound that features a benzene ring with a methyl group and a sulfur-containing side chain. This side chain is characterized by two ethoxyethyl groups attached to a sulfur atom, classifying it as an organosulfur compound. Its unique structure, which includes functional groups that are reactive in organic synthesis, renders it a valuable component in the chemical industry.

Uses

Used in Pharmaceutical Industry:
[(2,2-diethoxyethyl)sulfanyl]methylbenzene is used as a building block for the synthesis of various pharmaceuticals due to its organosulfur content and reactive functional groups. Its ability to be incorporated into the molecular structures of drugs makes it a versatile component in the development of new medications.
Used in Pesticide Industry:
In the pesticide industry, [(2,2-diethoxyethyl)sulfanyl]methylbenzene is utilized as a key component in the creation of different pesticides. Its chemical properties allow it to be tailored to target specific pests while minimizing environmental impact.
Used in Materials Science:
The sulfur-containing moiety of [(2,2-diethoxyethyl)sulfanyl]methylbenzene also makes it a candidate for applications in materials science. It can be used in the development of novel materials with specific properties, such as those with enhanced thermal or chemical stability, depending on the requirements of various applications.
Used in Organic Synthesis:
As a fundamental component in organic synthesis, [(2,2-diethoxyethyl)sulfanyl]methylbenzene is used as an intermediate for the production of a wide range of fine chemicals. Its unique structure allows for further functionalization and the creation of more complex molecules for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 91905-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,0 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91905-68:
(7*9)+(6*1)+(5*9)+(4*0)+(3*5)+(2*6)+(1*8)=149
149 % 10 = 9
So 91905-68-9 is a valid CAS Registry Number.

91905-68-9SDS

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 2,2-diethoxyethylsulfanylmethylbenzene

1.2 Other means of identification

Product number -
Other names benzylsulfanyl-acetaldehyde diethyl acetal

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:91905-68-9 SDS

91905-68-9Relevant articles and documents

Synthesis and properties of alkylthioethanals

Keiko, Natalia A.,Stepanova, Ludmila G.,Verochkina, Ekaterina A.,Chuvashev, Yurii A.

experimental part, p. 127 - 138 (2011/10/04)

A method, allowing alkylthioethanals to be synthesized in 80-93% yields, has been developed. It comprises the hydrolysis of bis-1,1-alkoxy-2- alkylthioethanes using two-phase system water - organic solvent. The method is applicable for both common aldehyd

Building units for N-backbone cyclic peptides. Part 4. Synthesis of protected Nα-functionalized alkyl amino acids by reductive alkylation of natural amino acids

Bitan, Gal,Muller, Dan,Kasher, Ron,Gluhov, Evgenia V.,Gilon, Chaim

, p. 1501 - 1510 (2007/10/03)

A new method for the synthesis of protected Nα-(ω-Y-alkyl) amino acids (Y is a thio, amino or carboxy group) and related compounds by reductive alkylation of natural amino acids is reported. These new amino acids serve as building units for the synthesis of backbone-cyclic peptides. They are orthogonally protected at the α-amino position by butoxycarbonyl (Boc) or 9-fluorenylmethoxycarbonyl (Fmoc), using trimethylsilyl temporary protection, to allow for their incorporation into peptides by solid phase peptide synthesis.

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