926625-05-0 Usage
Description
Methyl 3-(3-bromophenyl)-2,2-dimethylpropionate is a chemical compound with a molecular formula C13H17BrO2. It is a methyl ester derivative of 3-(3-bromophenyl)-2,2-dimethylpropionic acid and is commonly used in organic synthesis and pharmaceutical research. methyl 3-(3-bromophenyl)-2,2-dimethylpropionate is a clear, colorless liquid with a faint, sweet odor and is soluble in organic solvents such as ethanol, acetone, and chloroform.
Uses
Used in Pharmaceutical Research:
Methyl 3-(3-bromophenyl)-2,2-dimethylpropionate is used as a building block in the synthesis of various pharmaceutical compounds for its versatile reactivity and functional group compatibility.
Used in Agrochemical Compounds:
Methyl 3-(3-bromophenyl)-2,2-dimethylpropionate is also utilized in the synthesis of agrochemical compounds, contributing to the development of new pesticides and other agricultural products.
Used in Organic Synthesis:
methyl 3-(3-bromophenyl)-2,2-dimethylpropionate is used as an intermediate in organic synthesis, allowing for the creation of a wide range of organic molecules for various applications.
It is important to handle methyl 3-(3-bromophenyl)-2,2-dimethylpropionate with care as it is considered hazardous if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 926625-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,6,2 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 926625-05:
(8*9)+(7*2)+(6*6)+(5*6)+(4*2)+(3*5)+(2*0)+(1*5)=180
180 % 10 = 0
So 926625-05-0 is a valid CAS Registry Number.
926625-05-0Relevant articles and documents
SUBSTITUTED, SATURATED AND UNSATURATED N-HETEROCYCLIC CARBOXAMIDES AND RELATED COMPOUNDS FOR THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS
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Paragraph 00474, (2021/04/01)
The invention provides substituted, saturated and unsaturated N-heterocyclic carboxamides and related compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat medical disorders, e.g., cancer, lysosomal storage disorder, neurodegenerative disorder, inflammatory disorder, in a patient.
Highly regioselective carbonylation of unactivated C(sp3)-H bonds by ruthenium carbonyl
Hasegawa, Nao,Charra, Valentine,Inoue, Satoshi,Fukumoto, Yoshiya,Chatani, Naoto
supporting information; experimental part, p. 8070 - 8073 (2011/07/08)
The regioselective carbonylation of unactivated C(sp3)-H bonds of aliphatic amides was achieved using Ru3(CO)12 as a catalyst. The presence of a 2-pyridinylmethylamine moiety in the amide is crucial for a successful reaction. The reaction shows a preference for C-H bonds of methyl groups as opposed to methylene C-H bonds and tolerates a variety of functional groups. The stoichiometric reaction of an amide with Ru 3(CO)12 gave a dinuclear ruthenium complex in which the 2-pyridinylmethylamino moiety was coordinated to the ruthenium center in an N,N manner.
