16181-14-9 Usage
Appearance
Yellow-brown oily liquid The compound has a yellow-brown color and exhibits an oily liquid consistency.
Molecular weight
229.57 g/mol The molecular weight of 1-bromo-4-[(2-chloroethyl)sulfanyl]benzene is 229.57 grams per mole.
Usage
Synthesis of pharmaceuticals and agrochemicals This chemical compound is utilized in the production of various pharmaceutical and agrochemical products.
Potential applications
Organic chemistry 1-bromo-4-[(2-chloroethyl)sulfanyl]benzene has potential applications in the field of organic chemistry, although specific uses are not mentioned.
Classification
Bromoalkylthio compound The compound is classified as a bromoalkylthio compound, which means it contains a bromine atom and a sulfanyl group.
Structure
Benzene ring with a bromine atom and a chloroethylsulfanyl group The compound's structure features a benzene ring with a bromine atom attached at the 1-position and a chloroethylsulfanyl group at the 4-position.
Industrial uses
Potential The chemical has potential industrial uses, although specific applications are not provided.
Precautions
Toxic and hazardous properties 1-bromo-4-[(2-chloroethyl)sulfanyl]benzene should be handled with caution due to its toxic and hazardous nature.
Check Digit Verification of cas no
The CAS Registry Mumber 16181-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,8 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16181-14:
(7*1)+(6*6)+(5*1)+(4*8)+(3*1)+(2*1)+(1*4)=89
89 % 10 = 9
So 16181-14-9 is a valid CAS Registry Number.
16181-14-9Relevant articles and documents
A highly efficient carbon-sulfur bond formation reaction via microwave-assisted nucleophilic substitution of thiols to polychloroalkanes without a transition-metal catalyst
Cao, Yi-Ju,Lai, Yuan-Yuan,Cao, Hong,Xing, Xiao-Ning,Wang, Xiang,Xiao, Wen-Jing
, p. 1529 - 1533 (2007/10/03)
An efficient carbon-sulfur bond formation reaction has been developed under microwave irradiation. This reaction affords a novel and rapid synthesis of thioacetals and sulfides under mild conditions. This method is particularly noteworthy given its experimental simplicity and high generality, and no transition-metal catalysts were needed under our conditions.
