93994-16-2 Usage
Benzene derivative
Yes
This compound is a derivative of benzene, with additional functional groups attached to the benzene ring.
Functional groups
tert-butyl group, phenylethynylsulfanyl group
The compound has a tert-butyl group (C4H9) and a phenylethynylsulfanyl group (C6H5C≡CSH2) attached to the benzene ring.
Use in organic synthesis
Building block
1-tert-butyl-4-[(phenylethynyl)sulfanyl]benzene is commonly used as a building block in organic synthesis for the preparation of various organic compounds.
Applications
Pharmaceutical and agrochemical production
This chemical is used in the production of pharmaceuticals and agrochemicals.
Physical state at room temperature
Solid
The compound is a solid at room temperature.
Solubility
Insoluble in water
1-tert-butyl-4-[(phenylethynyl)sulfanyl]benzene is insoluble in water.
Handling and storage
Cool, dry place, away from heat and flame
This chemical should be handled with care and stored in a cool, dry place, away from sources of heat and flame to prevent accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 93994-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,9 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93994-16:
(7*9)+(6*3)+(5*9)+(4*9)+(3*4)+(2*1)+(1*6)=182
182 % 10 = 2
So 93994-16-2 is a valid CAS Registry Number.
93994-16-2Relevant articles and documents
Radical-mediated sulfonyl alkynylation, allylation, and cyanation of propellane
Wu, Zhen,Xu, Yaohui,Zhang, Huihui,Wu, Xinxin,Zhu, Chen
supporting information, p. 6066 - 6069 (2021/06/21)
Bicyclo[1.1.1]pentane (BCP) is widely applied as the bioisostere for aryl, internal alkynes, andtert-butyl groups in medicinal chemistry. We herein disclose an efficient and practical preparation of sulfonyl alkynyl/allyl/cyano-substituted BCP derivatives
