76542-19-3 Usage
Structure
Benzene derivative with a bromine atom and a propylthio group attached to the benzene ring
Explanation
The compound is derived from benzene, which is a six-carbon ring with alternating single and double bonds. A bromine atom is attached to one of the carbons in the ring, and a propylthio group (a three-carbon chain with a sulfur atom at the end) is attached to another carbon in the ring.
Explanation
The bromine atom and propylthio group are the functional groups in this compound, which give it its unique chemical properties and reactivity.
Explanation
1-bromo-4-(propylthio)Benzene is used as a starting material or intermediate in the synthesis of a wide range of organic compounds, particularly in the pharmaceutical and agrochemical industries. It is also used as a building block for creating polymers and other industrial chemicals.
Explanation
Due to its potential hazards, it is essential to follow safety guidelines and precautions when working with 1-bromo-4-(propylthio)Benzene. This may include wearing appropriate personal protective equipment (PPE), working in a well-ventilated area, and following proper disposal and storage procedures.
Functional Groups
Bromine atom, Propylthio group
Applications
Intermediate in the synthesis of various organic compounds, pharmaceutical and agrochemical industries, building block in the production of polymers and other industrial chemicals
Hazardous Chemical
Proper safety precautions should be taken when handling and working with it
Check Digit Verification of cas no
The CAS Registry Mumber 76542-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76542-19:
(7*7)+(6*6)+(5*5)+(4*4)+(3*2)+(2*1)+(1*9)=143
143 % 10 = 3
So 76542-19-3 is a valid CAS Registry Number.
76542-19-3Relevant articles and documents
Enantioselective nitrene transfer to sulfides catalyzed by a chiral iron complex
Wang, Jun,Frings, Marcus,Bolm, Carsten
supporting information, p. 8661 - 8665 (2013/09/12)
Iron works: Enantioselective nitrene transfer to sulfide was accomplished by a chiral iron(III)/PyBOX catalyst (see scheme). Various sulfimides were thus obtained in high enantioselectivities and yields. Applications of this protocol to the syntheses of enantioenriched sulfoximines and an epoxide were also demonstrated. Copyright
2-AZA-BICYCLO[2.2.2]OCTANE COMPOUNDS AND USES THEREOF
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Page/Page column 77, (2010/08/09)
This invention relates to 2-aza-bicyclo [2.2.2] octane compounds (and salts thereof), the process for making such a compound and pharmaceutical compositions comprising such a compound. The invention also relates to the use of the compounds for modulating
THERAPEUTIC AGENTS
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Page/Page column 39, (2008/06/13)
A compound of the formula (I): wherein R1,R2,R3, R4,Ar, A, n and m are defined herein, is disclosed as a GlyT1 inhibitor; pharmaceutical compositions containing the compound of the formula (I) are also disclosed as are their use in medicine, for example in the treatment of schizophrenia.
