156450-83-8 Usage
Explanation
The compound is composed of 10 carbon atoms, 13 hydrogen atoms, 1 bromine atom, 3 oxygen atoms, and 1 sulfur atom.
Explanation
The compound is based on a benzene ring, which is a six-membered carbon ring with alternating single and double bonds.
Explanation
The compound has two functional groups attached to the benzene ring a bromopropoxy group (C3H7OBr) and a methylsulfonyl group (CH3SO2).
Explanation
This group consists of a bromine atom (Br) attached to a propoxy chain, which is a three-carbon (C3H7) chain with an oxygen atom (O) at the end.
Explanation
This group consists of a methyl group (CH3) attached to a sulfonyl group (SO2), which is a sulfur dioxide (SO2) molecule.
Explanation
The compound is commonly used in the synthesis of various organic compounds and may have potential applications in the development of pharmaceuticals and agrochemicals.
Explanation
Based on the molecular size and complexity, it is reasonable to assume that the compound is a liquid or solid at room temperature, although specific data on its physical state is not provided.
Explanation
The compound's functional groups, particularly the bromopropoxy and methylsulfonyl groups, make it susceptible to various types of chemical reactions, including nucleophilic substitution, elimination, and addition reactions.
Explanation
As a brominated compound, 1-(3-bromopropoxy)-4-(methylsulfonyl)benzene may pose health risks, such as being an irritant or toxic, and should be handled with care in a laboratory setting.
Structure
Benzene derivative
Functional groups
Bromopropoxy and methylsulfonyl
Bromopropoxy group
C3H7OBr
Methylsulfonyl group
CH3SO2
Applications
Organic synthesis, pharmaceutical, and agrochemical industries
Physical state
Likely a liquid or solid at room temperature
Solubility
Likely soluble in organic solvents
Reactivity
May undergo substitution, elimination, and addition reactions
Hazards
Potential irritant or toxic
Check Digit Verification of cas no
The CAS Registry Mumber 156450-83-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,4,5 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156450-83:
(8*1)+(7*5)+(6*6)+(5*4)+(4*5)+(3*0)+(2*8)+(1*3)=138
138 % 10 = 8
So 156450-83-8 is a valid CAS Registry Number.
156450-83-8Relevant articles and documents
Transition metal- And light-free radical borylation of alkyl bromides and iodides using silane
Mo, Fanyang,Sun, Beiqi,Zheng, Sihan
supporting information, p. 5674 - 5677 (2021/06/16)
We report operationally simple and neutral conditions for borylation of alkyl bromides and iodides to alkyl boronic esters under transition metal- and light-free conditions. A series of substrates with a wide range of functional groups were effectively transformed into the borylation products in moderate to good yields. Mechanistic studies, including radical clock experiments and DFT calculations, gave detailed insight into the radical borylation process.
SUBSTITUTED BENZOIC ACIDS, INHIBITORS OF PHOSPHOLIPASES A2
-
, (2008/06/13)
The compounds of formula I are potent inhibitors of phospholipases A 2 (PLA 2 's) and are therefore useful in the treatment of diseases, such as psoriasis, inflammatory bowel disease, asthma, allergy, arthritis, dermatitis, gout, pulmonary disease, myocardial ischemia, and trauma induced inflammation, such as spinal cord injury.
