27006-02-6 Usage
Description
4-Bromo-3,5-dimethylbenzyl alcohol, also known as 3,5-dimethyl-4-bromobenzyl alcohol, is a chemical compound with the formula C9H11BrO. It is a white to light yellow solid that exhibits a strong odor. This versatile compound is widely used in the pharmaceutical and chemical industries as an intermediate or starting material for the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Industry:
4-Bromo-3,5-dimethylbenzyl alcohol is used as an intermediate or starting material for the synthesis of different types of drugs, particularly benzodiazepines. Benzodiazepines are a class of psychoactive drugs known for their sedative, hypnotic, and anxiolytic properties.
Used in Chemical Industry:
4-BroMo-3,5-diMethylbenzyl alcohol is also utilized as a reagent in the production of various organic compounds, contributing to the development of new chemical entities and processes.
Used in Flavors and Fragrances Industry:
4-Bromo-3,5-dimethylbenzyl alcohol is an important building block in the synthesis of flavors and fragrances, making it a valuable compound in the field of organic chemistry. Its unique properties and reactivity allow for the creation of a wide range of scent and taste profiles, enhancing the sensory experience of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 27006-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,0 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27006-02:
(7*2)+(6*7)+(5*0)+(4*0)+(3*6)+(2*0)+(1*2)=76
76 % 10 = 6
So 27006-02-6 is a valid CAS Registry Number.
27006-02-6Relevant articles and documents
Oxidation of Iodo- and Bromo-Substituted Polymethylbenzenes in the System PbO2–CF3COOH–CH2Cl2
Sandzhieva,Aryamova,Sukharzhevskii,Grinenko,Vasilyev
, p. 397 - 402 (2018/06/12)
The oxidation of mono- and diiodo- and -bromo-substituted polymethylbenzenes (mesitylene and durene) in the system PbO2–CF3COOH–CH2Cl2 at room temperature (2–70 h) leads mainly to the formation of iodo- and brom
ANTIDIABETIC TRICYCLIC COMPOUNDS
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Page/Page column 97, (2015/04/28)
Novel compounds of the structural formula (I), and the pharmaceutically acceptable salts thereof, are agonists of G-protein coupled receptor 40 (GPR40) and may be useful in the treatment, prevention and suppression of diseases mediated by the G-protein-coupled receptor 40. The compounds of the present invention may be useful in the treatment of Type 2 diabetes mellitus, and of conditions that are often associated with this disease, including obesity and lipid disorders, such as mixed or diabetic dyslipidemia, hyperlipidemia, hypercholesterolemia, and hypertriglyceridemia.
Total synthesis of pterosines B and C via a photochemical key step
Wessig, Pablo,Teubner, Janek
, p. 1543 - 1546 (2007/10/03)
A total synthesis of pterosines B and C is reported. Starting with a fourfold substituted benzene derivative, the introduction of the remaining substituents is mainly based on Sonogashira couplings followed by different transformations of the ethyne moiety. The key step is a photochemical ring-closure of an α-mesyloxy ketone forming the 1-indanone skeleton. Georg Thieme Verlag Stuttgart.
