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1795-04-6

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1795-04-6 Usage

General Description

2,3,5-Trimethylthiophene is a chemical compound with the molecular formula C7H8S. It is a colorless to pale yellow liquid with a strong, sweet odor. 2,3,5-Trimethylthiophene is mainly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of fragrances and flavorings. Additionally, it has applications in the manufacturing of polymers and as a chemical intermediate in organic synthesis. The compound is known for its potential as a fragrance and is considered to be an aromatic compound with an appealing aroma. However, it should be handled and stored with care, as it may pose health and environmental risks if not managed properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1795-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1795-04:
(6*1)+(5*7)+(4*9)+(3*5)+(2*0)+(1*4)=96
96 % 10 = 6
So 1795-04-6 is a valid CAS Registry Number.

1795-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-TRIMETHYLTHIOPHENE

1.2 Other means of identification

Product number -
Other names Trimethylthiophene

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:1795-04-6 SDS

1795-04-6Relevant articles and documents

Synthesis and structure of novel disulfide(trisulfide)-containing thiophenes

Deng, Shi-Ren,Wu, Tao,Hu, Gao-Qiang,Li, Dan,Zhou, Yun-Hong,Li, Zao-Ying

, p. 71 - 78 (2007)

A novel trisulfide-containing thiophene, 1,5-dihydrothieno[3,4-e][1,2,3] trithiepine (5), and a disulfide analogue, 1,4-dihydrothieno[3,4-d][1,2]dithiine (4), were designed and synthesized. All the compounds were characterized by FT-IR, NMR, Raman, MS, an

Reaction of dimethyl disulfide with thiophene catalyzed by zeolite

Mashkina,Khairulina

, (2015)

Reaction of dimethyl disulfide with thiophene under the action of highly siliceous zeolite at 180-350°C and contact time 0.6-14 s resulted in formation of thioalkylation products, 2-(methylsulfanyl)- and 2,5-bis(methylsulfanyl)thiophenes and also alkylate

Catalytic reactions of dimethyl disulfide with thiophene and benzene

Mashkina,Khairulina

, p. 72 - 81 (2016/04/20)

The gas-phase reaction of dimethyl disulfide with thiophene proceeds under the action of acid catalysts under atmospheric pressure at 160-350°C and a residence time of τ = 0.6-21 s to form thioalkylation and alkylation products. Dimethyl disulfide reacts with benzene to form only alkylation products. Catalysts containing both strong protic and Lewis acid sites, as well as basic sites of moderate strength, are the most active ones.

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