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5718-74-1

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5718-74-1 Usage

Chemical class

Thiophene A class of organic compounds containing a five-membered ring of four carbon atoms and one sulfur atom.

Bicyclic structure

Two interconnected rings The compound has two rings that are connected to each other.

Molecular weight

150.26 g/mol The mass of one mole of the compound is 150.26 grams.

Unique and complex structure

Useful in various applications The compound's structure makes it valuable in pharmaceutical, agrochemical, and material science industries.

Reactivity

Valuable building block The compound's properties and reactivity make it a useful starting point for the synthesis of other organic compounds.

Substituents

1,3,3-trimethyl The compound has three methyl groups (CH3) attached to the bicyclic structure, specifically at the 1st, 3rd, and 3rd positions.

Presence of sulfur

Thiabicyclo[2.2.2]octane The compound contains a sulfur atom in its bicyclic structure, which contributes to its unique properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 5718-74-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5718-74:
(6*5)+(5*7)+(4*1)+(3*8)+(2*7)+(1*4)=111
111 % 10 = 1
So 5718-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H18S/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3

5718-74-1SDS

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 2,2,4-trimethyl-3-thiabicyclo[2.2.2]octane

1.2 Other means of identification

Product number -
Other names EINECS 227-218-0

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:5718-74-1 SDS

5718-74-1Relevant articles and documents

Generation of VBr? VBi? VO?? defect clusters for 1O2 production for molecular oxygen activation in photocatalysis

Ding, Jie,Dai, Zan,Tian, Fan,Zhou, Bo,Zhao, Bin,Zhao, Huiping,Chen, Zhiquan,Liu, Yunling,Chen, Rong

supporting information, p. 23453 - 23459 (2017/11/30)

Defect engineering on a semiconductor surface can provide coordinatively unsaturated sites for molecular oxygen activation in photocatalysis. In this work, we demonstrated that the vacancy type was key to modulate the molecular oxygen activation process on BiOBr nanosheets. By regulating the reaction time, an oxygen vacancy (VO??), a double atom defect cluster (VBi? VO??) and triple atom clusters (VBi? VO?? VBi? and VBr? VBi? VO??) were accordingly generated on the surface, subsurface and bulk of BiOBr. More importantly, the newly-discovered VBr? VBi? VO?? defect cluster was highly related to the singlet oxygen (1O2) production ability of BiOBr. Meanwhile, the excellent photocatalytic selective oxidation reactions were successfully realized over BiOBr with the VBr? VBi? VO?? defect cluster. In addition, time-dependent defect cluster generation and the associated molecular oxygen activation were discussed.

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