81613-58-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 6 hydrogen (H) atoms, 1 bromine (Br) atom, and 6 fluorine (F) atoms.
Explanation
The compound is derived from benzene, which is a six-carbon ring with alternating single and double bonds. It has a propynyl group (a three-carbon chain with a triple bond at one end and a bromine atom attached to the middle carbon) and two trifluoromethyl groups (-CF3) attached to the benzene ring.
Explanation
The functional groups in this compound are the propynyl group and the two trifluoromethyl groups. These groups give the compound its unique chemical properties and reactivity.
Explanation
The compound is used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable building block for creating new molecules with specific functions.
Explanation
The compound's distinct chemical structure and properties make it a valuable tool for researchers and industrial applications in the field of organic chemistry. It can be used to develop new materials and technologies with specific properties and functions.
Explanation
Due to its unique structure and properties, the compound is a valuable tool for researchers working in organic chemistry. It can be used to study reaction mechanisms, develop new synthetic methods, and create novel compounds with potential applications in various industries.
Structure
Benzene derivative with a bromine-substituted propynyl group and two trifluoromethyl groups attached to the benzene ring
Functional Groups
Propynyl, Trifluoromethyl
Application
Organic synthesis and building block for pharmaceuticals and agrochemicals
Unique Properties
Useful in the development of new materials and technologies
Industrial Applications
Valuable tool for researchers in the field of organic chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 81613-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,1 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81613-58:
(7*8)+(6*1)+(5*6)+(4*1)+(3*3)+(2*5)+(1*8)=123
123 % 10 = 3
So 81613-58-3 is a valid CAS Registry Number.
81613-58-3Relevant articles and documents
Novel 5-(3-aryl-2-propynyl)-5-(arylsulfonyl)thiazolidine-2,4-diones as antihyperglycemic agents
Wrobel, Jay,Li, Zenan,Dietrich, Arlene,McCaleb, Michael,Mihan, Brenda,Sredy, Janet,Sullivan, Donald
, p. 1084 - 1091 (2007/10/03)
Novel 5-(3-aryl-2-propynyl)-5-(arylsulfonyl)thiazolidine-2,4-diones and 5-(3-aryl-2-propynyl)5-(arylsulfanyl)thiazolidine-2,4-diones were prepared and evaluated as oral antihyperglycemic agents in the obese, insulin resistant db/db mouse model at 100 mg/kg and, if the analogue had sufficient potency, 20 mg/kg. The sulfonylthiazolidinediones, 2, were more potent than the corresponding sulfanylthiazolidinedione congeners, 1. With regard to substituent effects on the 3-propynyl phenyl ring (Ar') of 2, 4-halogen substitution generally resulted in the more potent analogues. Substituent effects on the phenylsulfonyl moiety (Ar) of 2 were less clear, although para-halogen substitution on Ar generally was preferable. 2-Pyridinesulfonyl derivatives (Ar = 2-pyridine in 2) also had good potency. Several compounds from series 2 were effective at lowering glucose and insulin in the obese, insulin resistant ob/ob mouse at the 50 mg/kg oral dose. Compound 20 significantly improved the glucose tolerance of obese, insulin resistant Zucker rats at the 20 mg/kg dose level and had no effect on plasma glucose or on glucose tolerance in normal rats fasted for 18 h at the 100 mg/kg level.
Rodenticidal 1-(3,5-bistrifluoromethylphenyl)-3-(4-t-butylpiperidino)prop-1-yne
-
, (2008/06/13)
The hitherto unknown phenylpropargylamine derivative 1-(3,5-bistrifluoromethylphenyl)-3-(4-tert-butylpiperidino)prop-1-yne, and acid addition salts thereof, have been found to be useful for killing warm-blooded vermin, especially rodents. Processes for the preparation of the new phenylpropargylamine derivative are described and so are suitable rodenticidal compositions.
